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Phenotypic and molecular characterization of Bruck syndrome (osteogenesis imperfecta with contractures of the large joints) caused by a recessive mutation in PLOD2

✍ Scribed by Russia Ha-Vinh; Yasemin Alanay; Ruud A. Bank; Ana Belinda Campos-Xavier; Andreas Zankl; Andrea Superti-Furga; Luisa Bonafé


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
154 KB
Volume
131A
Category
Article
ISSN
1552-4825

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