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Common mutation in the PHKA2 gene with variable phenotype in patients with liver phosphorylase b kinase deficiency

✍ Scribed by Samira Achouitar; Jennifer L. Goldstein; Miski Mohamed; Stephanie Austin; Keri Boyette; Francoise M. Blanpain; Catherine W. Rehder; Priya S. Kishnani; Saskia B. Wortmann; Martin den Heijer; Dirk J. Lefeber; Ron A. Wevers; Deeksha S. Bali; Eva Morava

Book ID: 116989427
Publisher: Elsevier Science
Year: 2011
Tongue: English
Weight: 152 KB
Volume: 104
Category: Article
ISSN: 1096-7192
DOI: 10.1016/j.ymgme.2011.08.021

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