A homozygous missense variant in the alkaline phosphatase gene ALPL is associated with a severe form of canine hypophosphatasia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-018-37801-2.pdf
Reference73 articles.
1. Bonafe, L. et al. Nosology and classification of genetic skeletal disorders: 2015 revision. Am. J. Med. Genet. A. 167A, 2869–2892 (2015).
2. Rathbun, J. C. Hypophosphatasia; a new developmental anomaly. Am. J. Dis. Child. 75, 822–831 (1948).
3. Whyte, M. P. Hypophosphatasia - aetiology, nosology, pathogenesis, diagnosis and treatment. Nat. Rev. Endocrinol. 12, 233–246 (2016).
4. Weiss, M. J. et al. Isolation and characterization of a cDNA encoding a human liver/bone/kidney-type alkaline phosphatase. Proc. Natl. Acad. Sci. USA 83, 7182–7186 (1986).
5. Weiss, M. J. et al. A missense mutation in the human liver/bone/kidney alkaline phosphatase gene causing a lethal form of hypophosphatasia. Proc. Natl. Acad. Sci. USA 85, 7666–7669 (1988).
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