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Teriparatide Treatment in Patients withWNT1orPLS3Mutation-Related Early-Onset Osteoporosis - A Pilot Study
Author(s) -
VilleValtteri Välimäki,
Outi Mäkitie,
Renata C. Pereira,
Christine Lainé,
Katherine WesselingPerry,
Jorma A. Määttä,
Mikko Kirjavainen,
Heli Viljakainen,
Matti Välimäki
Publication year - 2016
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.2016-2423
Subject(s) - medicine , teriparatide , osteoporosis , bone remodeling , endocrinology , n terminal telopeptide , bone mineral , femoral neck , urology , osteocalcin , chemistry , alkaline phosphatase , biochemistry , enzyme
We previously identified 2 Finnish families with dominantly inherited, low-turnover osteoporosis caused by mutations in WNT1 or PLS3.

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