Welander hereditary distal myopathy, a molecular genetic comparison to hereditary myopathies with inclusion bodies
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference16 articles.
1. Myopathia distalis tarda hereditaria;Welander;Acta Med Scand,1951
2. Distal myopathies. 25th ENMC International workshop, 18–20 November 1994, Naarden, The Netherlands;Somer;Neuromusc Disord,1995
3. Homozygous appearance of distal myopathy;Welander;Acta Genet,1957
4. Distribution of muscle degeneration in Welander distal myopathy – a magnetic resonance and muscle biopsy study;Åhlberg;Neuromusc Disord,1994
5. `Rimmed vacuole myopathy' sparing the quadriceps;Argov;J Neurol Sci,1984
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1. The Multifunctional Faces of T-Cell Intracellular Antigen 1 in Health and Disease;International Journal of Molecular Sciences;2022-01-26
2. A Heterologous Cell Model for Studying the Role of T-Cell Intracellular Antigen 1 in Welander Distal Myopathy;Molecular and Cellular Biology;2019-01
3. Welander distal myopathy is caused by a mutation in the RNA-binding protein TIA1;Annals of Neurology;2013-02-11
4. Evaluation of a Hand-training Programme for Patients with Welander Distal Myopathy;Scandinavian Journal of Occupational Therapy;2003-12
5. Refined mapping of the Welander distal myopathy region on chromosome 2p13 positions the new candidate region telomeric of the DYSF locus;Neurogenetics;2003-06-27
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