Autosomal centronuclear myopathy due to mutations in the skeletal muscle ryanodine receptor gene

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Author(s): Jungbluth H, Zhou H, Bertini E, Straub V, Bushby K, Robb S, Treves S, Sewry C, Muntoni F

Publication type: Conference Proceedings (inc. Abstract)

Publication status: Published

Conference Name: Annual Meeting of the British Paediatric Neurology Association

Year of Conference: 2006

Pages: 30-31

ISSN: 0012-1622

Publisher: Developmental Medicine and Child Neurology: Cambridge University Press

URL: http://dx.doi.org/10.1017/S001216220600017X

DOI: 10.1017/S001216220600017X

Notes: Abstract 60

Library holdings: Search Newcastle University Library for this item

ISBN:

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