A mutation in theHSN2gene causes sensory neuropathy type II in a Lebanese family-Reference-Cited by-同舟云学术

A mutation in theHSN2gene causes sensory neuropathy type II in a Lebanese family

Published:2004-09-28 Issue:4 Volume:56 Page:572-575
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Rivière Jean-Baptiste,Verlaan Dominique J.,Shekarabi Masoud,Lafrenière Ronald G.,Bénard Mélanie,Der Kaloustian Vazken M.,Shbaklo Zuhayr,Rouleau Guy A.

Funder

Canadian Institutes of Health Research

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference17 articles.

1. Hereditary sensory and autonomic neuropathies. Familial dysautonomia and other HSANs;Axelrod;Clin Auton Res,2002

2. Assessment and evaluation of hereditary sensory and autonomic neuropathies with autonomic and neurophysiological examinations;Hilz;Clin Auton Res,2002

3. SPTLC1 is mutated in hereditary sensory neuropathy, type 1;Bejaoui;Nat Genet,2001

4. Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I;Dawkins;Nat Genet,2001

5. The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3;Nicholson;Nat Genet,1996

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