Generation of Isogenic D4Z4 Contracted and Noncontracted Immortal Muscle Cell Clones from a Mosaic Patient-Reference-Cited by-同舟云学术

Generation of Isogenic D4Z4 Contracted and Noncontracted Immortal Muscle Cell Clones from a Mosaic Patient

Published:2012-10 Issue:4 Volume:181 Page:1387-1401
ISSN:0002-9440
Container-title:The American Journal of Pathology
language:en
Short-container-title:The American Journal of Pathology

Author:

Krom Yvonne D.,Dumonceaux Julie,Mamchaoui Kamel,den Hamer Bianca,Mariot Virginie,Negroni Elisa,Geng Linda N.,Martin Nicolas,Tawil Rabi,Tapscott Stephen J.,van Engelen Baziel G.M.,Mouly Vincent,Butler-Browne Gillian S.,van der Maarel Silvère M.

Publisher

Elsevier BV

Subject

Pathology and Forensic Medicine

Reference63 articles.

1. Facioscapulohumeral muscular dystrophy;Tawil;Muscle Nerve,2006

2. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy;Wijmenga;Nat Genet,1992

3. Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: implications for genetic counselling and etiology of FSHD1;van Deutekom;Hum Mol Genet,1996

4. Epigenetic mechanisms of facioscapulohumeral muscular dystrophy;de Greef;Mutat Res,2008

5. Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy;van Overveld;Nat Genet,2003

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