Clinical Practice Guidelines for Hypophosphatasia*

Hypophosphatasia (HPP) is a rare bone disease caused by inactivating mutations in the ALPL gene, which encodes tissue-nonspecific alkaline phosphatase (TNSALP). Patients with HPP have varied clinical manifestations and are classified based on the age of onset and severity. Recently, enzyme replaceme...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Clin Pediatr Endocrinol
Main Authors: Michigami, Toshimi, Ohata, Yasuhisa, Fujiwara, Makoto, Mochizuki, Hiroshi, Adachi, Masanori, Kitaoka, Taichi, Kubota, Takuo, Sawai, Hideaki, Namba, Noriyuki, Hasegawa, Kosei, Fujiwara, Ikuma, Ozono, Keiichi
Formato: Artigo
Idioma:Inglês
Publicado em: The Japanese Society for Pediatric Endocrinology 2020
Assuntos:
Special Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6958520/
https://ncbi.nlm.nih.gov/pubmed/32029969
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1297/cpe.29.9
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados