WNK1/HSN2founder mutation in patients with hereditary sensory and autonomic neuropathy: A Japanese cohort study-Reference-Cited by-同舟云学术

WNK1/HSN2founder mutation in patients with hereditary sensory and autonomic neuropathy: A Japanese cohort study

Published:2017-07-20 Issue:6 Volume:92 Page:659-663
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Yuan J.-H.¹^ORCID,Hashiguchi A.¹,Yoshimura A.¹^ORCID,Sakai N.²,Takahashi M.P.³,Ueda T.⁴,Taniguchi A.⁵,Okamoto S.⁶,Kanazawa N.⁷,Yamamoto Y.⁷,Saigoh K.⁸,Kusunoki S.⁸,Ando M.¹,Hiramatsu Y.¹,Okamoto Y.¹,Takashima H.¹

Affiliation:

1. Department of Neurology and Geriatrics; Kagoshima University, Graduate School of Medical and Dental Sciences; Kagoshima Japan

2. Child Healthcare and Genetic Science Laboratory, Division of Health Science; Osaka University, Graduate School of Medicine; Osaka Japan

3. Department of Functional Diagnostic Science, Division of Health Science; Osaka University, Graduate School of Medicine; Osaka Japan

4. Division of Neurology; Kobe University, Graduate School of Medicine; Kobe Japan

5. Department of Neurology; Mie University, Graduate School of Medicine; Mie Japan

6. Department of Rehabilitation Medicine; Fujita Health University, Nanakuri Memorial Hospital; Mie Japan

7. Department of Dermatology; Wakayama Medical University; Wakayama Japan

8. Department of Neurology; Kindai University, Faculty of Medicine; Osaka Japan

Funder

Nervous and Mental Disorders and Research Committee for Charcot-Marie-Tooth Disease, Neuropathy, Ataxic Disease and Applying Health

Technology of Ministry of Health, Welfare and Labour, Japan

Japan Agency for Medical Research and Development

JSPS KAKENHI

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.13037/fullpdf

Reference17 articles.

1. Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates;Lafreniere;Am J Hum Genet,2004

2. A mutation in the HSN2 gene causes sensory neuropathy type II in a Lebanese family;Riviere;Ann Neurol,2004

3. Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians;Roddier;Neurology,2005

4. Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type II;Coen;Neurology,2006

5. New HSN2 mutation in Japanese patient with hereditary sensory and autonomic neuropathy type 2;Takagi;Neurology,2006

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