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C4342T-mutation in the SCN4A gene on chromosome 17q in a Swedish family with paramyotonia congenita (Eulenburg) – correlations with clinical, neurophysiological and muscle biopsy data

✍ Scribed by Kristian Borg; Gabrielle Åhlberg; Maria Anvret


Book ID
117670600
Publisher
Elsevier Science
Year
1997
Tongue
English
Weight
90 KB
Volume
7
Category
Article
ISSN
0960-8966

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