Hereditary Motor and Sensory Neuropathy Mutation

Hereditary Motor and Sensory Neuropathy Mutation

A duplication in chromosome 17 responsible for most cases of autosomal dominant HMSN 1 was present as a de-novo mutation in 9 out of 10 sporadic patients examined at the Department of Neurology, Academic Medical Center, Amsterdam, The Netherlands.

Bibliographic Details
Main Author:	J Gordon Millichap
Format:	Article
Language:	English
Published:	Pediatric Neurology Briefs Publishers 1992-06-01
Series:	Pediatric Neurology Briefs
Subjects:	de-novo mutation autosomal recessive genetic loci
Online Access:	https://www.pediatricneurologybriefs.com/articles/3011

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