SEPN1: Associated with congenital fiber-type disproportion and insulin resistance-Reference-Cited by-同舟云学术

SEPN1: Associated with congenital fiber-type disproportion and insulin resistance

Published:2006-03 Issue:3 Volume:59 Page:546-552
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Clarke Nigel F.,Kidson Warren,Quijano-Roy Susana,Estournet Brigitte,Ferreiro Ana,Guicheney Pascale,Manson James I.,Kornberg Andrew J.,Shield Lloyd K.,North Kathryn N.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference15 articles.

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2. Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease: reassessing the nosology of early-onset myopathies;Ferreiro;Am J Hum Genet,2002

4. The spectrum of the so-called rigid spine syndrome: nosological considerations and report of three female cases;Bertini;J Neurol,1986

5. Multi-minicore disease-searching for boundaries: phenotype analysis of 38 cases;Ferreiro;Ann Neurol,2000

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