Muscle fiber-type selective propensity to pathology in the nmd mouse model of SMARD1
Author:
Funder
National Institute of Health
NIH PREP
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference37 articles.
1. The natural course of infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1);Eckart;Pediatrics,2012
2. Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1;Grohmann;Nat. Genet.,2001
3. Diaphragmatic spinal muscular atrophy with respiratory distress is heterogeneous, and one form Is linked to chromosome 11q13-q21;Grohmann;Am. J. Hum. Genet.,1999
4. The wide spectrum of clinical phenotypes of spinal muscular atrophy with respiratory distress type 1: a systematic review;Porro;J. Neurol. Sci.,2014
5. Infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1);Grohmann;Ann. Neurol.,2003
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