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                                       Details for article 32 of 36 found articles
 
 
  Severe phenotypes of paralysis periodica paramyotonia are associated with the Met1592Val mutation in the voltage-gated sodium channel gene (SCN4A) in a Chinese family
 
 
Title: Severe phenotypes of paralysis periodica paramyotonia are associated with the Met1592Val mutation in the voltage-gated sodium channel gene (SCN4A) in a Chinese family
Author: Feng, Yu
Ji, Xinping
Sun, Xiaohong
Wang, Hong
Zhang, Chaodong
Appeared in: Journal of clinical neuroscience
Paging: Volume 18 (2011) nr. 8 pages 3 p.
Year: 2011
Contents:
Publisher: Elsevier Ltd
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 32 of 36 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands