Associated Papers
Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss.
Bakhchane A et al.
Plos One, 2017
28472130 (PubMed )
Supplement: pone.0176516.s002.xlsx › Feuil1
Analysis of the GIGYF2 gene in familial and sporadic Parkinson disease in the Spanish population.
Samaranch L et al.
European Journal of Neurology, 2010
GIGYF2 mutations are not a frequent cause of familial Parkinson's disease.
Di Fonzo A et al.
Parkinsonism & Related Disorders, 2009
Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson disease.
Lautier C et al.
American Journal of Human Genetics, 2008
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