Variable phenotypes are associated with PMP22 missense mutations-Reference-Cited by-同舟云学术

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Variable phenotypes are associated with PMP22 missense mutations

Published:2011-02 Issue:2 Volume:21 Page:106-114
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Russo M.,Laurá M.,Polke J.M.,Davis M.B.,Blake J.,Brandner S.,Hughes R.A.C.,Houlden H.,Bennett D.L.H.,Lunn M.P.T.,Reilly M.M.

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference29 articles.

1. Diagnosis and new treatments in genetic neuropathies;Reilly;J Neurol Neurosurg Psychiatr,2009

2. Sorting out the inherited neuropathies;Reilly;Pract Neurol,2007

3. DNA duplication associated with Charcot-Marie-Tooth disease type 1A;Lupski;Cell,1991

4. Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a);Raeymaekers;Neuromuscul Disord,1991

5. DNA deletion associated with hereditary neuropathy with liability to pressure palsies;Chance;Cell,1993

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