Identification of a Novel Gene (HSN2) Causing Hereditary Sensory and Autonomic Neuropathy Type II through the Study of Canadian Genetic Isolates-Reference-Cited by-同舟云学术

Identification of a Novel Gene (HSN2) Causing Hereditary Sensory and Autonomic Neuropathy Type II through the Study of Canadian Genetic Isolates

Published:2004-05 Issue:5 Volume:74 Page:1064-1073
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Lafrenière Ronald G.,MacDonald Marcia L.E.,Dubé Marie-Pierre,MacFarlane Julie,O’Driscoll Mary,Brais Bernard,Meilleur Sébastien,Brinkman Ryan R.,Dadivas Owen,Pape Terry,Platon Christèle,Radomski Chris,Risler Jenni,Thompson Jay,Guerra-Escobio Ana-Maria,Davar Gudarz,Breakefield Xandra O.,Pimstone Simon N.,Green Roger,Pryse-Phillips William,Goldberg Y. Paul,Younghusband H. Banfield,Hayden Michael R.,Sherrington Robin,Rouleau Guy A.,Samuels Mark E.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference36 articles.

1. Familial dysautonomia is caused by mutations of the IKAP gene;Anderson;Am J Hum Genet,2001

2. Hereditary sensory and autonomic neuropathies: familial dysautonomia and other HSANs;Axelrod;Clin Auton Res,2002

3. Four siblings with type II hereditary sensory and autonomic neuropathy;Basu;Indian Pediatr,2002

4. SPTLC1 is mutated in hereditary sensory neuropathy, type I;Bejaoui;Nat Genet,2001

5. WNK1, a kinase mutated in inherited hypertension with hyperkalemia, localizes to diverse Cl- -transporting epithelia;Choate;Proc Natl Acad Sci USA,2003

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