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Seminars in Pediatric Neurology
Volume 12, Issue 3
, Pages 152-158
, September 2005
The Dystroglycanopathies: The New Disorders of O-Linked Glycosylation
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POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker Warburg syndrome
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Supported by grants from the Muscular Dystrophy Association and the National Institutes of Health (AR050202) to PTM.
PII: S1071-9091(05)00076-8
doi: 10.1016/j.spen.2005.10.003
© 2005 Elsevier Inc. All rights reserved.
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Seminars in Pediatric Neurology
Volume 12, Issue 3
, Pages 152-158
, September 2005
