X-linked Emery–Dreifuss muscular dystrophy manifesting with adult onset axial weakness, camptocormia, and minimal joint contractures-Reference-Cited by-同舟云学术

X-linked Emery–Dreifuss muscular dystrophy manifesting with adult onset axial weakness, camptocormia, and minimal joint contractures

Published:2019-09 Issue:9 Volume:29 Page:678-683
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Brisset Marion,Ben Yaou Rabah,Carlier Robert-Yves,Chanut Anaїs,Nicolas Guillaume,Romero Norma B.,Wahbi Karim,Decrocq Camille,Leturcq France,Laforêt Pascal,Malfatti Edoardo

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference22 articles.

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2. Identification of a novel X-linked gene responsible for Emery–Dreifuss muscular dystrophy;Bione;Nat Genet,1994

3. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery–Dreifuss muscular dystrophy;Bonne;Nat Genet,1999

4. Emerin in health and disease;Koch;Semin Cell Dev Biol,2014

5. Emery–Dreifuss muscular dystrophy, laminopathies, and other nuclear envelopathies;Bonne,2013

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