Toggle Main Menu Toggle Search

Open Access padlockePrints

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

Downloads

Full text for this publication is not currently held within this repository. Alternative links are provided below where available.


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

ISBN:


Share