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Different missense mutations at the tissue-nonspecific alkaline phosphatase gene locus in autosomal recessively inherited forms of mild and severe hypophosphatasia.

Hypophosphatasia is a heritable form of rickets/osteomalacia with extremely variable clinical expression. Severe forms are inherited in an autosomal recessive fashion; the mode of transmission of mild forms is uncertain. The biochemical hallmark of hypophosphatasia is deficient activity of the tissu...

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Bibliografische Detailangaben
Veröffentlicht in:Proc Natl Acad Sci U S A
Hauptverfasser: Henthorn, P S, Raducha, M, Fedde, K N, Lafferty, M A, Whyte, M P
Format: Artigo
Sprache:Inglês
Veröffentlicht: National Academy of Sciences 1992
Schlagworte:
Online-Zugang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC50246/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1409720/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.89.20.9924
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