Mosaic caveolin-3 expression in acquired rippling muscle disease without evidence of myasthenia gravis or acetylcholine receptor autoantibodies-Reference-Cited by-同舟云学术

Mosaic caveolin-3 expression in acquired rippling muscle disease without evidence of myasthenia gravis or acetylcholine receptor autoantibodies

Published:2011-03 Issue:3 Volume:21 Page:194-203
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Lo Harriet P.,Bertini Enrico,Mirabella Massimiliano,Domazetovska Ana,Dale Russell C.,Petrini Stefania,D’Amico Adele,Valente Enza Maria,Barresi Rita,Roberts Mark,Tozzi Giulia,Tasca Giorgio,Cooper Sandra T.,Straub Volker,North Kathryn N.

Publisher

Elsevier BV

Subject

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

Reference33 articles.

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2. Caveolinopathies: mutations in caveolin-3 cause four distinct autosomal dominant muscle diseases;Woodman;Neurology,2004

3. Severe autosomal recessive rippling muscle disease;Koul;Muscle Nerve,2001

4. Autosomal recessive rippling muscle disease with homozygous CAV3 mutations;Kubisch;Ann Neurol,2005

5. Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy;Hayashi;J Clin Invest,2009

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