Author:
Masi Laura,Brandi Maria Luisa
Publisher
Springer Nature Switzerland
Reference47 articles.
1. Anderson HC. Molecular biology of matrix vesicles. Clin Orthop Relat Res. 1995;314:266–80.
2. Baumgartner-Sigl SB, Haberlandt E, Mumm S, et al. Pyridoxine-responsive seizures as the first symptom of infantile hypophosphatasia caused by two novel missense mutations (c.677T>C, p.M226T; c.1112C>T,p.T371I) of the tissue-nonspecific alkaline phosphatase gene. Bone. 2007;40:1655–61.
3. Berseth KE, Tebben PJ, Drake MT, et al. Clinical spectrum of hypophosphatasia diagnosed in adults. Bone. 2013;54:21–7.
4. Bishop N. Clinical management of hypophosphatasia. Clin Cases Miner Bone Metab. 2015;12:170–3.
5. Fauvert D, Brun-Heath I, Lia-Baldini AS, et al. Mild forms of hypophosphatasia mostly result from dominant negative effect of severe alleles or from compound heterozygosity for severe and moderate alleles. BMC Med Genet. 2009;10:51.