Charcot-Marie-Tooth disease due to a de novo mutation of the RAB7 gene.

Article Details

Citation

Meggouh F, Bienfait HM, Weterman MA, de Visser M, Baas F

Charcot-Marie-Tooth disease due to a de novo mutation of the RAB7 gene.

Neurology. 2006 Oct 24;67(8):1476-8.

PubMed ID
17060578 [ View in PubMed
]
Abstract

We report a 32-year-old patient with Charcot-Marie-Tooth (CMT2B) including foot ulcerations. Genetic analysis identified a de novo mutation in the small GTP-ase late endosomal RAB7 gene, consisting of a c.471G>C, p.Lys157Asn missense mutation. This observation strongly supports the hypothesis that RAB7 mutations are responsible for CMT2B.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Serine palmitoyltransferase 1O15269Details
Ras-related protein Rab-7aP51149Details