|
rs61752717
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Specifically, the data from our American series are insufficient to evaluate the hypothesis that the M694V/M694V genotype confers a more severe phenotype, or increases the risk of amyloidosis; but both our data and the recent literature (160) indicate that amyloidosis can occur in FMF patients with only 1 copy, or no copies, of the M694V mutation.
|
9715731 |
1998 |
|
rs3743930
|
|
|
0.800 |
GeneticVariation |
BEFREE |
Nevertheless, E148Q helps account for recessive inheritance in an Ashkenazi family previously reported as an unusual case of dominantly inherited FMF.
|
10090880 |
1999 |
|
rs61752717
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Homozygosity for the M694V mutation, predominant among North African Jews, is associated with a severe course and prognosis for FMF.
|
10224214 |
1999 |
|
rs61752717
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis.
|
10234504 |
1999 |
|
rs61752717
|
|
|
0.900 |
GeneticVariation |
BEFREE |
MEFV-Gene analysis in armenian patients with Familial Mediterranean fever: diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic implications.
|
10364520 |
1999 |
|
rs11466024
|
|
|
0.840 |
GeneticVariation |
BEFREE |
Eight mutations, one of which (R408Q) is new, were found to account for 93% of the 163 independent FMF alleles, with both FMF alleles identified in 89% of the patients.
|
10364520 |
1999 |
|
rs61752717
|
|
|
0.900 |
GeneticVariation |
BEFREE |
The discovery of the gene responsible for FMF, Mediterranean fever gene (MEFV), and of associated mutations represents a major advance that now allows researchers to establish a strong, although nonexclusive association between one specific mutation, M694V, and the amyloid phenotype.
|
10647956 |
2000 |
|
rs61752717
|
|
|
0.900 |
GeneticVariation |
BEFREE |
A Turkish patient with episodic fever and thoracic pain is described in whom a homozygous M694V mutation of the MEFV gene confirmed the clinical diagnosis of familial Mediterranean fever.
|
10667038 |
2000 |
|
rs28940578
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Recently, the gene responsible for FMF, MEFV, has been cloned and four missense mutations (M680I, M694V, V726A and M694I) have been described.
|
10709887 |
2000 |
|
rs28940580
|
|
|
0.890 |
GeneticVariation |
BEFREE |
Recently, the gene responsible for FMF, MEFV, has been cloned and four missense mutations (M680I, M694V, V726A and M694I) have been described.
|
10709887 |
2000 |
|
rs3743930
|
|
|
0.800 |
GeneticVariation |
BEFREE |
Among the parents group (obligatory carriers), in addition to the 2 parents that were homozygous E148Q, in 2 families one of the parents was heterozygote for E148Q but transmitted the other allele (apparently with unknown FMF mutation) to the affected child.
|
10737995 |
2000 |
|
rs61752717
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Sixty-five patients clinically diagnosed as having FMF underwent molecular genetic studies using polymerase chain reaction and restriction endonuclease digestion methods to detect the presence of the 4 mutations (M694V, V726A, M680I, M694I).
|
10852276 |
2000 |
|
rs61752717
|
|
|
0.900 |
GeneticVariation |
BEFREE |
These results provide evidence that FMF patients without the M694V mutation are also at risk for the development of amyloidosis.
|
10905662 |
2000 |
|
rs767006697
|
|
|
0.010 |
GeneticVariation |
BEFREE |
There was no statistically significant difference between healthy controls and FMF patients for the Ala138Gly polymorphism (p=0.9).
|
11139244 |
2001 |
|
rs61752717
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694I mutations.
|
11175300 |
2001 |
|
rs61752717
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Study of the mutation M694V of familial Mediterranean fever in Jews.
|
11336402 |
2001 |
|
rs3743930
|
|
|
0.800 |
GeneticVariation |
BEFREE |
Five founder mutations, V726A, M694V, M694I, M680I and E148Q account for 74% of FMF chromosomes from typical cases (Armenians, Arabs, Jews, and Turks).
|
11464238 |
2001 |
|
rs61752717
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Both were found in compound heterozygosity with the mutation M694V in single Turkish patients with clinical syndromes characteristic for FMF.
|
11470495 |
2001 |
|
rs3743930
|
|
|
0.800 |
GeneticVariation |
BEFREE |
Six sequence alterations (M694V, V726A, K695R, M680I, M694I, and E148Q), in the MEFV gene, account for the majority of FMF chromosomes.
|
11977178 |
2002 |
|
rs61752717
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Cranial nerve lesions and abnormal visually evoked potentials associated with the M694V mutation in familial Mediterranean fever.
|
12189462 |
2002 |
|
rs61752717
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Two hundred sixteen children who met the clinical criteria for FMF underwent molecular genetic studies to detect the 3 most common mutations in the Israeli FMF patient population (M694V, V726A, E148Q).
|
12508410 |
2003 |
|
rs3743930
|
|
|
0.800 |
GeneticVariation |
BEFREE |
Two hundred sixteen children who met the clinical criteria for FMF underwent molecular genetic studies to detect the 3 most common mutations in the Israeli FMF patient population (M694V, V726A, E148Q).
|
12508410 |
2003 |
|
rs61752717
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Male sex coupled with articular manifestations cause a 4-fold increase in susceptibility to amyloidosis in patients with familial Mediterranean fever homozygous for the M694V-MEFV mutation.
|
12563686 |
2003 |
|
rs61752717
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Pulmonary manifestations during FMF attacks are significantly more common in the Jewish population bearing the M694V mutation.
|
12746942 |
2003 |
|
rs61752717
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Several mutations have been identified of which the homozygous form of the M694V mutation is associated with a more severe expression of FMF.
|
12781406 |
2003 |