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Article

Evidence that abnormal high bone mineralization in growing children with osteogenesis imperfecta is not associated with specific collagen mutations.

Calcified tissue international - 1 Apr 2008

Roschger Paul, Fratzl-Zelman Nadja, Misof Barbara M, Glorieux Francis H, Klaushofer Klaus, Rauch Frank

Abstract excerpt

Osteogenesis imperfecta type I (OI-I) represents the mildest form of OI. The collagen I mutations underlying the disorder can be classified as quantitative mutations that lead to formation of a decreased amount of normal collagen or qualitative mutations where structurally aberrant collagen chain...

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Source

Identifiers

PMID: 18311573
DOI: 10.1007/s00223-008-9113-x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18311573-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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