Severe phenotypes of paralysis periodica paramyotonia are associated with the Met1592Val mutation in the voltage-gated sodium channel gene (SCN4A) in a Chinese family

✍ Scribed by Yu Feng; Xinping Ji; Xiaohong Sun; Hong Wang; Chaodong Zhang

• Book ID: 116676059
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 386 KB
• Volume: 18
• Category: Article
• ISSN: 0967-5868
• DOI: 10.1016/j.jocn.2010.12.035