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Mutation analyses in 17 patients with deficiency in acid β-galactosidase: three novel point mutations and high correlation of mutation W273L with Morquio disease type B

✍ Scribed by Eduard Paschke; Ivica Milos; Heidemarie Kreimer-Erlacher; Gerald Hoefler; Michael Beck; Maria Hoeltzenbein; Wim Kleijer; Thierry Levade; Helen Michelakakis; B. Radeva

Publisher: Springer
Year: 2001
Tongue: English
Weight: 130 KB
Volume: 109
Category: Article
ISSN: 0340-6717
DOI: 10.1007/s004390100570

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