A congenital myopathy with diaphragmatic weakness not linked to the SMARD1 locus-Reference-Cited by-同舟云学术

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A congenital myopathy with diaphragmatic weakness not linked to the SMARD1 locus

Published:2007-02 Issue:2 Volume:17 Page:174-179
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Hartley L.,Kinali M.,Knight R.,Mercuri E.,Hubner C.,Bertini E.,Manzur A.Y.,Jimenez-Mallebrera C.,Sewry C.A.,Muntoni F.

Publisher

Elsevier BV

Subject

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

Reference23 articles.

1. Severe infantile neuropathy with diaphragmatic weakness and its relationship to SMARD1;Pitt;Brain,2003

2. Myotubular myopathy: morphological, immunohistochemical and clinical variation;Helliwell;Neuromuscul Disord,1998

3. Infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1);Grohmann;Ann Neurol,2003

4. Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1;Grohmann;Nat Genet,2001

5. Diaphragmatic paralysis due to spinal muscular atrophy. An unrecognised cause of respiratory failure in infancy?;McWilliam;Arch Dis Child,1985

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