The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease

2001/12/17 by Ana Cuesta, Laia Pedrola, Teresa Sevilla +11 · 297 citations
Biochemistry, Genetics and Molecular Biology · Neuroscience · #Allele #Biology #Gene #Genetics #Hereditary Neurological Disorders #Locus (genetics) #Mutant #Mutation #Neurological diseases and metabolism #Nuclear Structure and Function #Phenotype #Tooth disease

paper · doi:10.1038/ng798

published in Nature Genetics 30(1), 22-25 (Springer Science and Business Media LLC)

crossref issued 2001/12/17 · crossref published 2001/12/17 · crossref published-online 2001/12/17 · openalex publication_date 2001/12/17 · crossref published-print 2002/01/01 · crossref created 2002/07/26 · crossref deposited 2023/05/18 · openalex created_date 2025/10/10 · crossref indexed 2026/06/29 · openalex updated_date 2026/07/26

Citations

• Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21

Cited by

• Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21
• GDAP1, the protein causing Charcot–Marie–Tooth disease type 4A, is expressed in neurons and is associated with mitochondria
• Mutations in the ganglioside-induced differentiation-associated protein-1 (GDAP1) gene in intermediate type autosomal recessive Charcot-Marie-Tooth neuropathy
• Genetics of Charcot-Marie-Tooth disease type 4A: mutations, inheritance, phenotypic variability, and founder effect
• Mutations in GDAP1
• GDAP1 [wikipedia]