Diaphragmatic dysfunction in SEPN1-related myopathy-Reference-Cited by-同舟云学术

Diaphragmatic dysfunction in SEPN1-related myopathy

Published:2017-08 Issue:8 Volume:27 Page:747-755
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Caggiano Serena,Khirani Sonia,Dabaj Ivana,Cavassa Eliana,Amaddeo Alessandro,Arroyo Jorge Olmo,Desguerre Isabelle,Richard Pascale,Cutrera Renato,Ferreiro Ana,Estournet Brigitte,Quijano-Roy Susana,Fauroux Brigitte

Publisher

Elsevier BV

Subject

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

Reference29 articles.

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3. Early onset myopathy with a novel mutation in the Selenoprotein N gene (SEPN1);Tajsharghi;Neuromuscul Disord,2005

5. Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome;Moghadaszadeh;Nat Genet,2001

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