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Severe muscle–eye–brain disease is associated with a homozygous mutation in the POMGnT1 gene

✍ Scribed by Serap Teber; Taner Sezer; Mehpare Kafalı; M. Chiara Manzini; Berrin Konuk Yüksel; Mustafa Tekin; Suat Fitöz; Christopher A. Walsh; Gülhis Deda

Book ID: 113590243
Publisher: Elsevier Science
Year: 2008
Tongue: English
Weight: 427 KB
Volume: 12
Category: Article
ISSN: 1090-3798
DOI: 10.1016/j.ejpn.2007.06.008

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