E Udd… - 2011 - books.google.com Copyright Ó 2011 by John Wiley & Sons, Inc. All rights reserved. Published by John Wiley & Sons, Inc., Hoboken, New Jersey Published simultaneously in Canada No part of this publication may be reproduced, stored in a retrieval system, or transmitted in any form or by any ... Cited by 297 - Related articles - All 6 versions
…, JE Landers, RH Brown Jr, B Udd… - American journal of …, 2011 - ncbi.nlm.nih.gov Linkage analysis of the dominant distal myopathy we previously identified in a large Australian family demonstrated one significant linkage region located on chromosome 7 and encompassing 18.6 Mbp and 151 genes. The strongest candidate gene was FLNC because filamin C, ...
…, T Suominen, S Penttilä, B Udd… - Acta Neurologica …, 2011 - Wiley Online Library ... How to Cite. Hilbert, P., Frank, S., Raheem, O., Suominen, T., Penttilä, S., Udd, B. and Fischer, D. (2011), Normal muscle MRI does not preclude increased connective tissue in muscle of recessive myotonia congenita. Acta Neurologica Scandinavica, 124: 146–147. ... All 2 versions
…, D Auboeuf, L Garcia, P Zimmermann, B Udd… - Nature Medicine, 2011 - nature.com Myotonic dystrophy is the most common muscular dystrophy in adults and the first recognized example of an RNA-mediated disease. Congenital myotonic dystrophy (CDM1) and myotonic dystrophy of type 1 (DM1) or of type 2 (DM2) are caused by the expression of mutant ... Cited by 3 - All 3 versions
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