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                                       Details for article 18 of 28 found articles
 
 
  Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene
 
 
Title: Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene
Author: Zhou, Haiyan
Lillis, Suzanne
Loy, Ryan E.
Ghassemi, Farshid
Rose, Michael R.
Norwood, Fiona
Mills, Kerry
Al-Sarraj, Safa
Lane, Russell J.M.
Feng, Lucy
Matthews, Emma
Sewry, Caroline A.
Abbs, Stephen
Buk, Stefan
Hanna, Michael
Treves, Susan
Dirksen, Robert T.
Meissner, Gerhard
Muntoni, Francesco
Jungbluth, Heinz
Appeared in: Neuromuscular disorders
Paging: Volume 20 (2010) nr. 3 pages 8 p.
Year: 2010
Contents:
Publisher: Elsevier B.V.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 18 of 28 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands