Compound heterozygous mutations of the TNXB gene cause primary myopathy. Response
Neuromuscul Disord
.
2014 Jan;24(1):89.
doi: 10.1016/j.nmd.2013.10.008.
Epub 2013 Nov 6.
Authors
Valérie Allamand
1
,
Philippe Beurrier
2
,
Ludovic Martin
3
,
Fransiska Malfait
4
,
Delfien Syx
4
,
Anne DePaepe
4
Affiliations
1
Inserm, U974, Paris, France; CNRS, UMR7215, Paris, France; UPMC Univ Paris 06 UM76, Institut de Myologie, Paris, France. Electronic address: v.allamand@institut-myologie.org.
2
Centre de traitement de l'Hémophilie, Centre Hospitalier Universitaire d'Angers, France.
3
Service de Dermatologie, Centre Hospitalier Universitaire d'Angers, France.
4
Center for Medical Genetics, Ghent University Hospital, Belgium.
PMID:
24295814
DOI:
10.1016/j.nmd.2013.10.008
No abstract available
Publication types
Letter
Comment
MeSH terms
Humans
Male
Muscular Diseases / genetics*
Mutation / genetics*
Tenascin / genetics*
Substances
Tenascin