A genetic model for muscle–eye–brain disease in mice lacking protein O-mannose 1,2-N-acetylglucosaminyltransferase (POMGnT1)-Reference-Cited by-同舟云学术

A genetic model for muscle–eye–brain disease in mice lacking protein O-mannose 1,2-N-acetylglucosaminyltransferase (POMGnT1)

Published:2006-03 Issue:3 Volume:123 Page:228-240
ISSN:0925-4773
Container-title:Mechanisms of Development
language:en
Short-container-title:Mechanisms of Development

Author:

Liu Jianmin,Ball Sherry L.,Yang Yuan,Mei Pinchao,Zhang Lei,Shi Haining,Kaminski Henry J.,Lemmon Vance P.,Hu Huaiyu

Publisher

Elsevier BV

Subject

Developmental Biology,Embryology

Reference43 articles.

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3. Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker–Warburg syndrome;Beltran-Valero de Bernabe;J. Med. Genet.,2004

4. An adhesion molecule involved in muscular dystrophies: structural and functional analysis of dystroglycan domains;Brancaccio;Ital. J. Biochem.,2003

5. Dystrophic phenotype induced in vitro by antibody blockade of muscle alpha-dystroglycan–laminin interaction;Brown;J. Cell Sci.,1999

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