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HUMAN MUTATION, ISSN 1059-7794, 07/2014, Volume 35, Issue 7, pp. 868 - 879
Laing early onset distal myopathy and myosin storage myopathy are caused by mutations of slow skeletal/-cardiac myosin heavy chain encoded by the gene MYH7, as... 
Laing distal myopathy | FIBER-TYPE DISPROPORTION | HEAVY-CHAIN | MPD1 | SEQUENCE VARIATION | CARDIOMYOPATHY | DISEASE | GENETICS & HEREDITY | STORAGE MYOPATHY | MISSENSE MUTATIONS | MYH7 | Myosin | Muscles | Boycotts | Family | Genetic aspects | Muscle proteins | Muscular dystrophy | Musculoskeletal system | Mutation | Scoliosis | Cardiomyopathy
Journal Article
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 2016, Volume 26, Issue 9, pp. 598 - 603
Journal Article
Journal Article
NEUROMUSCULAR DISORDERS, ISSN 0960-8966, 02/2014, Volume 24, Issue 2, pp. 156 - 161
We describe a Hungarian Roma family originally investigated for autosomal dominant distal muscular atrophy. The mother started toe walking at 3 years and lost... 
Distal myopathy | Laing distal myopathy | PATHOLOGY | NEUROSCIENCES | BICD2 | CLINICAL NEUROLOGY | HYPERTROPHIC CARDIOMYOPATHY | SPINAL MUSCULAR-ATROPHY | Whole exome sequencing | MISSENSE MUTATION | Myosinopathies | MOTOR ADAPTER | LINKAGE | MYH7
Journal Article
Acta Neurologica Belgica, ISSN 0300-9009, 12/2014, Volume 114, Issue 4, pp. 253 - 256
We report the first Belgian family with Laing early-onset distal myopathy (MPD1). The proposita started limping at age 7. Later, there was severe weakness of... 
Neurology | Neurosciences | Biomedicine | Myosin immunohistochemistry | Laing early-onset distal myopathy | Distal myopathies | Medicine/Public Health, general | Neuroradiology | MYH7 | MUTATION | NEUROSCIENCES | CLINICAL NEUROLOGY
Journal Article
Journal of Clinical Neuromuscular Disease, ISSN 1522-0443, 03/2015, Volume 16, Issue 3, pp. 164 - 169
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 07/2018, Volume 115, Issue 28, pp. E6566 - E6575
Journal Article
Journal Article