Clinical and genetic characteristics of hypophosphatasia in Chinese children.

Orphanet J Rare Dis · 2021 · PMC8028151 · PMID 33827627

Europe PMC DOI

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an increasing trendno p-value reported

15/23 (65.22%) cases of the reported HPP were within the past three years, indicating an increasing trend of the awareness, detection, and diagnosis of HPP (Additional file 1 : Figure S1).

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