Back to Search Start Over

EP.23A novel LMNA mutation identified in an Argentinian patient with autosomal dominant Emery-Dreifuss muscular dystrophy phenotype

Authors :
C. Belziti
M. Bettini
C. Azcona
Marcelo Rugiero
M. Brogger
Source :
Neuromuscular Disorders. 29:S76-S77
Publication Year :
2019
Publisher :
Elsevier BV, 2019.

Subjects

Subjects :
Genetics
LMNA
Neurology
Pediatrics, Perinatology and Child Health
Mutation (genetic algorithm)
medicine
Neurology (clinical)
Biology
Emery–Dreifuss muscular dystrophy
medicine.disease
Phenotype
Genetics (clinical)

Details

ISSN :
09608966
Volume :
29
Database :
OpenAIRE
Journal :
Neuromuscular Disorders
Accession number :
edsair.doi...........84706d60883cf40fb6f177d04b4e2466
Full Text :
https://doi.org/10.1016/j.nmd.2019.06.153
Full Text Access
View/download PDF

Tools

Authors Abstract Subjects Details