Defective O-Glycosylation due to a Novel Homozygous S129P Mutation Is Associated with Lack of Fibroblast Growth Factor 23 Secretion and Tumoral Calcinosis

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language	eng
Author	Bergwitz Clemens Endocrine Unit (C.B., S.B., H.A.-Z., H.J.), Massachusetts General Hospital, Boston, Massachusetts 02114 Banerjee Santanu Endocrine Unit (C.B., S.B., H.A.-Z., H.J.), Massachusetts General Hospital, Boston, Massachusetts 02114 Abu-Zahra Hilal Endocrine Unit (C.B., S.B., H.A.-Z., H.J.), Massachusetts General Hospital, Boston, Massachusetts 02114 Kaji Hiroshi Division of Diabetes, Metabolism, and Endocrinology (H.K.), Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan Miyauchi Akimitsu Department of Medicine (A.M.), National Hyogo-Chuo Hospital, Hyogo 669-1515, Japan Sugimoto, Toshitsugu Jueppner Harald Endocrine Unit (C.B., S.B., H.A.-Z., H.J.), Massachusetts General Hospital, Boston, Massachusetts 02114 Pediatric Nephrology Unit (H.J.), Massachusetts General Hospital, Boston, Massachusetts 02114
Journal Title	JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Volume	94
Issue	11
Start Page	4267
End Page	4274
ISSN	0021-972X
ISSN（Online）	1945-7197
Published Date	2009-11
DOI	10.1210/jc.2009-0961
PubMed ID	19837926
Publisher	OXFORD UNIV PRESS INC
NII Type	Journal Article
OAI-PMH Set	Faculty of Medicine