Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2-Reference-Cited by-同舟云学术

Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2

Published:2014-12-14 Issue:2 Volume:138 Page:293-310
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Rossor Alexander M.,Oates Emily C.,Salter Hannah K.,Liu Yang,Murphy Sinead M.,Schule Rebecca,Gonzalez Michael A.,Scoto Mariacristina,Phadke Rahul,Sewry Caroline A.,Houlden Henry,Jordanova Albena,Tournev Iyailo,Chamova Teodora,Litvinenko Ivan,Zuchner Stephan,Herrmann David N.,Blake Julian,Sowden Janet E.,Acsadi Gyuda,Rodriguez Michael L.,Menezes Manoj P.,Clarke Nigel F.,Auer Grumbach Michaela,Bullock Simon L.,Muntoni Francesco,Reilly Mary M.,North Kathryn N.

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/138/2/293/11142859/awu356.pdf

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