Distinct contractile protein profile in congenital myotonic dystrophy and X-linked myotubular myopathy-Reference-Cited by-同舟云学术

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Distinct contractile protein profile in congenital myotonic dystrophy and X-linked myotubular myopathy

Published:1991-01 Issue:2 Volume:1 Page:103-111
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Soussi-Yanicostas N.,Chevallay M.,Laurent-Winter C.,Tomé F.M.S.,Fardeau M.,Butler-Browne G.S.

Publisher

Elsevier BV

Subject

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

Reference34 articles.

1. Sarcomeric myosin heavy chain is coded by a highly conserved multigene family;Nguyen,1982

2. Three myosin heavy chain isozymes appear sequentially in rat muscle development;Whalen;Nature,1981

3. Structural differences in the subfragment-1 and rod portions of myosin isozymes from adult and developing rat skeletal muscle;Bugaisky;J. Biol Chem,1984

4. Embryonic and fetal myosins in human skeletal muscle;Fitzsimons;J. Neurol Sci,1981

5. Myosin transitions in developing fast and slow muscles of rat hind limb;Lyons;Differentiation,1983

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1. Congenital Myopathies and Related Disorders;Muscle Biopsy;2021

2. Muscular Dystrophies and Allied Disorders V;Muscle Biopsy;2020

3. Congenital Myopathies and Related Diseases;Myopathology;2018-09-25

4. Myopathology in congenital myopathies;Neuropathology and Applied Neurobiology;2017-02

5. Skeletal Muscle Pathology in X-Linked Myotubular Myopathy: Review With Cross-Species Comparisons;Journal of Neuropathology & Experimental Neurology;2016-01-28

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