Periaxin mutations cause a broad spectrum of demyelinating neuropathies-Reference-Cited by-同舟云学术

Periaxin mutations cause a broad spectrum of demyelinating neuropathies

Published:2002-05-21 Issue:6 Volume:51 Page:709-715
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Takashima Hiroshi,Boerkoel Cornelius F.,De Jonghe Peter,Ceuterick Chantal,Martin Jean-Jacques,Voit Thomas,Schröder J.-Michael,Williams Anna,Brophy Peter J.,Timmerman Vincent,Lupski James R.

Funder

National Institute of Diabetes, Digestive, and Kidney Diseases

National Institutes of Health

National Institute of Neurological Disorders and Stroke

Muscular Dystrophy Association (J.R.L.)

Deutsche Forschungsgemeinschaft

University of Antwerp

Fund for Scientific Research (FWO-Flanders)

Born-Bunge Foundation (Sheid-van Bogaert Legacy)

Geneeskundige Stichting Koningin Elisabeth

Wellcome Trust

IMPULS (T.V.)

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference21 articles.

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2. Periaxin mutations cause recessive Dejerine-Sottas neuropathy;Boerkoel;Am J Hum Genet,2001

3. A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease;Guilbot;Hum Mol Genet,2001

4. Periaxin expression in myelinating Schwann cells: modulation by axon-glial interactions and polarized localization during development;Scherer;Development,1995

5. A tripartite nuclear localization signal in the PDZ-domain protein L-periaxin;Sherman;J Biol Chem,2000

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