Corrigendum to "Multigenerational genetic inheritance and clinical characteristics of the rare disease hypophosphatasia in 6 families: A case series" [Bone Rep. 26 (2025) 1-6 (101857)].
case_series · Level IV
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- Record sourced from PubMed, PMID 40977756.
- Also identified by DOI 10.1016/j.bonr.2025.101866 and PMC identifier 12447559.
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Abstract
[This corrects the article DOI: 10.1016/j.bonr.2025.101857.].