Confirmation that abnormal desmin accumulation and migration are due to a desmin gene mutation in a familial cardiomyopathy and distal myopathy.

Détails

Ressource 1Demande d'une copie Sous embargo indéterminé.
Accès restreint UNIL
Etat: Public
Version: Final published version
ID Serval
serval:BIB_0F81AEFE8A90
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
UNIL/CHUV
Titre
Confirmation that abnormal desmin accumulation and migration are due to a desmin gene mutation in a familial cardiomyopathy and distal myopathy.
Périodique
Neuromuscular disorders : NMD
Auteur⸱e⸱s
Dunand M., Lobrinus J.A., Jeannet P.Y., Behin A., Claeys K.G., Selcen D., Kuntzer T.
ISSN
1873-2364 (Electronic)
ISSN-L
0960-8966
Statut éditorial
Publié
Date de publication
11/2009
Peer-reviewed
Oui
Volume
19
Numéro
11
Pages
802
Langue
anglais
Notes
Publication types: Case Reports ; Letter
Publication Status: ppublish
PDF: Letter to the editor
Mots-clé
Adult, Aged, Cardiomyopathies/genetics, Cardiomyopathies/metabolism, Desmin/genetics, Desmin/metabolism, Distal Myopathies/genetics, Distal Myopathies/metabolism, Family Health, Female, Humans, Mutation
URN
urn:nbn:ch:serval-BIB_0F81AEFE8A909
OAI-PMH
oai:serval.unil.ch:BIB_0F81AEFE8A90
DOI
10.1016/j.nmd.2009.07.013
Pubmed
19716701
Web of science
000272020400014
Création de la notice
08/12/2009 16:55
Dernière modification de la notice
20/08/2019 13:36
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