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A single in-frame deletion in the CAPN3 gene is linked to muscular dystrophy with a dominant pattern of inheritance

Lookup NU author(s): Dr Richard Charlton, Professor Volker StraubORCiD, Professor Hanns Lochmuller, Emerita Professor Katherine Bushby, Dr Rita Barresi


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Publication metadata

Author(s): Henderson M, Hudson J, Marsh J, Charlton R, Straub V, Lochmuller H, Bushby K, Vissing J, Barresi R

Publication type: Conference Proceedings (inc. Abstract)

Publication status: Published

Conference Name: UK Neuromuscular Translational Research Conference

Year of Conference: 2012

Pages: S26-S26

ISSN: 0960-8966

Publisher: Pergamon

Library holdings: Search Newcastle University Library for this item

Series Title: Neuromuscular Disorders