Non-COL1A1/2 genetic burden and osteoporosis-overlap in patients referred with osteogenesis imperfecta phenotype.

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Bibliographic Details
Title: Non-COL1A1/2 genetic burden and osteoporosis-overlap in patients referred with osteogenesis imperfecta phenotype.
Authors: Ozturk FN; Department of Medical Genetics, Istanbul Haseki Education and Training Hospital, Haseki Training and Research Hospital, 34265, Sultangazi, Istanbul, Turkey. drnihaldilek@gmail.com., Keskin E; Department of Medical Genetics, Istanbul Haseki Education and Training Hospital, Haseki Training and Research Hospital, 34265, Sultangazi, Istanbul, Turkey.
Source: Archives of osteoporosis [Arch Osteoporos] 2026 Apr 30; Vol. 21 (1). Date of Electronic Publication: 2026 Apr 30.
Publication Type: Journal Article
Journal Info: Publisher: Springer Country of Publication: England NLM ID: 101318988 Publication Model: Electronic Cited Medium: Internet ISSN: 1862-3514 (Electronic) NLM ISO Abbreviation: Arch Osteoporos Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1862-3514
DOI:10.1007/s11657-026-01702-z