A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy-Reference-Cited by-同舟云学术

A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy

Published:2016-02-01 Issue:2 Volume:12 Page:e1005829
ISSN:1553-7404
Container-title:PLOS Genetics
language:en
Short-container-title:PLoS Genet

Author:

Hong Young Bin,Joo Jaesoon,Hyun Young Se,Kwak Geon,Choi Yu-Ri,Yeo Ha Kyung,Jwa Dong Hwan,Kim Eun Ja,Mo Won Min,Nam Soo Hyun,Kim Sung Min,Yoo Jeong Hyun,Koo Heasoo,Park Hwan Tae,Chung Ki Wha,Choi Byung-Ok

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics (clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

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4. Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease;H Houlden;Neuromolecular Med,2006

5. Basic neurochemistry;P Morell,1999

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