SLC25A13
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Clinical findings in five Turkish patients with citrin deficiency and identification of a novel mutation on SLC25A13.
|
31809266 |
2020 |
SLC25A13
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Biallelic SLC25A13 mutations result in Citrin deficiency (CD).
|
30708027 |
2019 |
SLC25A13
|
0.200 |
Biomarker
|
disease |
BEFREE |
Identification of the genes responsible for adult-onset type II citrullinemia (CTLN2) and citrin protein function have enhanced our understanding of citrin deficiency.
|
31255436 |
2019 |
SLC25A13
|
0.200 |
Biomarker
|
disease |
BEFREE |
Pivotal role of inter-organ aspartate metabolism for treatment of mitochondrial aspartate-glutamate carrier 2 (citrin) deficiency, based on the mouse model.
|
30862943 |
2019 |
SLC25A13
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
A genetic analysis of solute carrier family 25, member 13 revealed the presence of a homozygous 851del4 mutation, and a diagnosis of citrin deficiency was made.
|
30591617 |
2019 |
SLC25A13
|
0.200 |
Biomarker
|
disease |
BEFREE |
In contrast, the estimated carrier frequencies for SLC25A13, which causes citrin deficiency, were much higher compared with the incidence rate.
|
30887117 |
2019 |
SLC25A13
|
0.200 |
Biomarker
|
disease |
BEFREE |
Two subjects did not present with NICCD, and were subsequently diagnosed later in life after their siblings presented with symptoms of citrin deficiency at one month of age and subsequently received a molecular diagnosis.
|
30181955 |
2018 |
SLC25A13
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
SLC25A13 c.1610_1612delinsAT mutation in an Indian patient and literature review of 79 cases of citrin deficiency for genotype-phenotype associations.
|
29787821 |
2018 |
SLC25A13
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Mutations in SLC25A13 cause citrin deficiency, which has three phenotypes: neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD), failure to thrive and dyslipidemia caused by citrin deficiency (FTTDCD) and adult-onset type 2 citrullinemia (CTLN2).
|
27829683 |
2017 |
SLC25A13
|
0.200 |
CausalMutation
|
disease |
CLINVAR |
[Analysis of clinical features and SLC25A13 gene mutations in a family affected with neonatal intrahepatic cholestasis].
|
27577219 |
2016 |
SLC25A13
|
0.200 |
CausalMutation
|
disease |
CLINVAR |
Molecular diagnosis of pediatric patients with citrin deficiency in China: SLC25A13 mutation spectrum and the geographic distribution.
|
27405544 |
2016 |
SLC25A13
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Molecular diagnosis of pediatric patients with citrin deficiency in China: SLC25A13 mutation spectrum and the geographic distribution.
|
27405544 |
2016 |
SLC25A13
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Citrin deficiency was suspected, and genomic DNA analysis revealed a mutation (IVS16ins3kb) in SLC25A13, which encodes a mitochondrial aspartate-glutamate carrier protein.
|
26109823 |
2015 |
SLC25A13
|
0.200 |
GeneticVariation
|
disease |
CLINVAR |
Clinical, molecular and functional investigation on an infant with neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD).
|
24586645 |
2014 |
SLC25A13
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
A novel mutation of the SLC25A13 gene in a Chinese patient with citrin deficiency detected by target next-generation sequencing.
|
24161253 |
2014 |
SLC25A13
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
This study aims to investigate the effect of a novel missense mutation on the aspartate/glutamate carrier (AGC) function of citrin protein, and to explore the aberrant transcript from c.615+5G>A in the same CD infant.
|
24586645 |
2014 |
SLC25A13
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Screening for five prevalent mutations of SLC25A13 gene in Guangdong, China: a molecular epidemiologic survey of citrin deficiency.
|
25110155 |
2014 |
SLC25A13
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Inspissated bile syndrome in an infant with citrin deficiency and congenital anomalies of the biliary tract and esophagus: identification and pathogenicity analysis of a novel SLC25A13 mutation with incomplete penetrance.
|
25216257 |
2014 |
SLC25A13
|
0.200 |
CausalMutation
|
disease |
CLINVAR |
Molecular analysis of SLC25A13 gene in human peripheral blood lymphocytes: Marked transcript diversity, and the feasibility of cDNA cloning as a diagnostic tool for citrin deficiency.
|
23022256 |
2012 |
SLC25A13
|
0.200 |
CausalMutation
|
disease |
CLINVAR |
Multiple ovarian antral follicles in a preterm infant with neonatal intrahepatic cholestasis caused by citrin deficiency: a clinical, genetic and transcriptional analysis.
|
22710133 |
2012 |
SLC25A13
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Eleven SLC25A13 mutations account for 95% of the mutant alleles in Japanese patients with citrin deficiency.
|
22277121 |
2012 |
SLC25A13
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
Analysis of SLC25A13 mutations, identification of dysmorphic erythrocytes, hepatobiliary scintigraphic imaging and investigation of post-NICCD clinical presentations were performed in a citrin-deficient cohort comprised of 51 cases of children diagnosed with citrin deficiency in a Chinese pediatric center.
|
21424115 |
2011 |
SLC25A13
|
0.200 |
GeneticVariation
|
disease |
CLINVAR |
[SLC25A13 gene analysis in neonates with intrahepatic cholestasis caused by citrin deficiency].
|
21507300 |
2011 |
SLC25A13
|
0.200 |
Biomarker
|
disease |
BEFREE |
Citrin deficiency (CD) is an autosomal recessive disorder with SLC25A13 as causative gene that encodes citrin, the liver-type aspartate/glutamate carrier isoform 2 (AGC2).
|
22095253 |
2011 |
SLC25A13
|
0.200 |
GeneticVariation
|
disease |
BEFREE |
SLC25A13 gene mutations cause citrin deficiency, which leads to neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD).
|
20927635 |
2011 |