POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes-Reference-Cited by-同舟云学术

POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes

Published:2007-11 Issue:4 Volume:363 Page:1033-1037
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Biancheri Roberta,Falace Antonio,Tessa Alessandra,Pedemonte Marina,Scapolan Sara,Cassandrini Denise,Aiello Chiara,Rossi Andrea,Broda Paolo,Zara Federico,Santorelli Filippo Maria,Minetti Carlo,Bruno Claudio

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference22 articles.

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4. Characterization of POMT2, a novel member of the PMT protein O-mannosyltransferase family specifically localized to the acrosome of mammalian spermatids;Willer;Glycobiology,2002

5. POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker–Warburg syndrome;van Reeuwijk;J. Med. Genet.,2005

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