Isolation and Characterization of the Mouse Ortholog of the Fukuyama-type Congenital Muscular Dystrophy Gene
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference16 articles.
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2. Are breaches in the glia limitans the primary cause of the micropolygyria in Fukuyama-type congenital muscular dystrophy (FCMD)? Pathological study of the cerebral cortex of an FCMD fetus;Nakano;Acta Neuropathol,1996
3. Pial–glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy;Yamamoto;Brain Dev,1997
4. Breached cerebral glia limitans–basal lamina complex in Fukuyama-type congenital muscular dystrophy;Saito;Acta Neuropathol,1999
5. An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy;Kobayashi;Nature,1998
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1. Restoration of the defect in radial glial fiber migration and cortical plate organization in a brain organoid model of Fukuyama muscular dystrophy;iScience;2021-10
2. Temporal requirement of dystroglycan glycosylation during brain development and rescue of severe cortical dysplasia via gene delivery in the fetal stage;Human Molecular Genetics;2018-01-19
3. Mouse fukutin deletion impairs dystroglycan processing and recapitulates muscular dystrophy;Journal of Clinical Investigation;2012-09-04
4. Congenital muscular dystrophies;Handbook of Clinical Neurology;2011
5. Basement membrane fragility underlies embryonic lethality in fukutin-null mice;Neurobiology of Disease;2005-06
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