Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness-Reference-Cited by-同舟云学术

Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness

Published:2006-11 Issue:5 Volume:60 Page:597-602
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Murakami Terumi,Hayashi Yukiko K.,Noguchi Satoru,Ogawa Megumu,Nonaka Ikuya,Tanabe Yuzo,Ogino Mieko,Takada Fumio,Eriguchi Makoto,Kotooka Norihiko,Campbell Kevin P.,Osawa Makiko,Nishino Ichizo

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference26 articles.

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2. Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan;Brockington;Am J Hum Genet,2001

3. Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome;Beltran-Valero de Bernabe;Am J Hum Genet,2002

4. Deficiency of alpha-dystroglycan in muscle-eye-brain disease;Kano;Biochem Biophys Res Commun,2002

5. Defective glycosylation in muscular dystrophy;Muntoni;Lancet,2002

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