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Annals of Neurology, ISSN 0364-5134, 01/2012, Volume 71, Issue 1, pp. 141 - 145
Journal Article
Journal Article
Journal Article
Nursing, ISSN 0360-4039, 07/2017, Volume 47, Issue 7, pp. 54 - 58
Journal Article
Journal Article
Journal Article
Clinical and Translational Science, ISSN 1752-8054, 02/2014, Volume 7, Issue 1, pp. 29 - 32
Journal Article
Journal of Clinical Neuroscience, ISSN 0967-5868, 2006, Volume 13, Issue 1, pp. 111 - 114
Journal Article
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, ISSN 1128-2460, 10/2011, Volume 30, Issue 2, pp. 127 - 132
Journal Article
Neurology India, ISSN 0028-3886, 12/2004, Volume 52, Issue 4, pp. 446 - 449
Limb girdle muscular dystrophy (LGMD) is a phenotypic expression of a heterogeneous group of diseases and sarcoglycanopathy is one of the causes of LGMD. There... 
Muscular Dystrophies, Limb-Girdle - diagnosis | Sarcoglycans - metabolism | Humans | Child, Preschool | Male | Sarcoglycans - deficiency | Biopsy | Adolescent | Female | Muscular Dystrophies, Limb-Girdle - etiology | Retrospective Studies | Muscle, Skeletal - pathology | Muscular Dystrophies, Limb-Girdle - pathology | Child | Index Medicus
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 2014, Volume 24, Issue 5, pp. 431 - 435
Abstract Limb-girdle muscular dystrophy primarily affects the muscles of the hips and shoulders (the “limb-girdle” muscles), although it is a heterogeneous... 
Neurology | DNAJB6 | Limb-girdle muscular dystrophy | Exome sequencing | GENE | TITIN |