Cargando…
Clinical and Genetic Characteristics of Hypophosphatasia in Chinese Adults
Hypophosphatasia (HPP) is an inherited disease caused by ALPL mutation, resulting in decreased alkaline phosphatase (ALP) activity and damage to bone and tooth mineralization. The clinical symptoms of adult HPP are variable, making diagnosis challenging. This study aims to clarify the clinical and g...
Autores principales: | Li, Xiang, Ren, Na, Wang, Ziyuan, Wang, Ya, Hu, Yunqiu, Hu, Weiwei, Gu, Jiemei, Hong, Wei, Zhang, Zhenlin, Wang, Chun |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10137706/ https://www.ncbi.nlm.nih.gov/pubmed/37107680 http://dx.doi.org/10.3390/genes14040922 |
Ejemplares similares
-
Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfecta
por: Zhang, Hao, et al.
Publicado: (2017) -
Clinical and genetic characteristics of hypophosphatasia in Chinese children
por: Liu, Meijuan, et al.
Publicado: (2021) -
Genetics Evaluation of Targeted Exome Sequencing in 223 Chinese Probands With Genetic Skeletal Dysplasias
por: Lv, Shanshan, et al.
Publicado: (2021) -
Clinical and Molecular Characterization and Discovery of Novel Genetic Mutations of Chinese Patients with COL2A1-related Dysplasia
por: Xu, Yang, et al.
Publicado: (2020) -
Vitamin D pathway gene variation rs3740165 is associated with serological uric acid levels in healthy Chinese women
por: Gu, Jiemei, et al.
Publicado: (2022)