×
Entrez Id:
3908
Gene Symbol:
LAMA2
LAMA2
0.500
GeneticVariation
disease
LHGDN
LAMA2 mRNA processing alterations generate a complete deficiency of laminin-alpha2 protein and a severe congenital muscular dystrophy.
18053718
2008
×
Entrez Id:
3908
Gene Symbol:
LAMA2
LAMA2
0.500
Biomarker
disease
BEFREE
We suggest that expression profiling will provide important information to improve our understanding of the molecular basis of laminin alpha-2 positive MDC .
17010933
2006
×
Entrez Id:
3908
Gene Symbol:
LAMA2
LAMA2
0.500
Biomarker
disease
LHGDN
Laminin alpha1 chain mediated reduction of laminin alpha2 chain deficient muscular dystrophy involves integrin alpha7beta1 and dystroglycan.
16504180
2006
×
Entrez Id:
3908
Gene Symbol:
LAMA2
LAMA2
0.500
Biomarker
disease
LHGDN
Prenatal diagnosis in laminin alpha2 chain (merosin)-deficient congenital muscular dystrophy: a collective experience of five international centers.
16084089
2005
×
Entrez Id:
3908
Gene Symbol:
LAMA2
LAMA2
0.500
GeneticVariation
disease
LHGDN
LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy.
15452315
2004
×
Entrez Id:
3908
Gene Symbol:
LAMA2
LAMA2
0.500
GeneticVariation
disease
LHGDN
Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency.
12552556
2003
×
Entrez Id:
3908
Gene Symbol:
LAMA2
LAMA2
0.500
AlteredExpression
disease
LHGDN
Laminin alpha2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant mice.
12609502
2003
×
Entrez Id:
3908
Gene Symbol:
LAMA2
LAMA2
0.500
GeneticVariation
disease
LHGDN
Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2, FCMD, MEB and CMD1B loci, in three Tunisian patients.
12467726
2003
×
Entrez Id:
3908
Gene Symbol:
LAMA2
LAMA2
0.500
GeneticVariation
disease
LHGDN
Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin).
11938437
2002
×
Entrez Id:
3908
Gene Symbol:
LAMA2
LAMA2
0.500
GeneticVariation
disease
BEFREE
Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skipping.
11287370
2001
×
Entrez Id:
3908
Gene Symbol:
LAMA2
LAMA2
0.500
GeneticVariation
disease
BEFREE
An early onset muscular dystrophy with diaphragmatic involvement, early respiratory failure and secondary alpha2 laminin deficiency unlinked to the LAMA2 locus on 6q22.
10726842
1998
×
Entrez Id:
3908
Gene Symbol:
LAMA2
LAMA2
0.500
GeneticVariation
disease
CLINVAR
×
Entrez Id:
3908
Gene Symbol:
LAMA2
LAMA2
0.500
Biomarker
disease
HPO