Novel ALPL genetic alteration associated with an odontohypophosphatasia phenotype.
about
The ever-expanding conundrum of primary osteoporosis: aetiopathogenesis, diagnosis, and treatment.Hypophosphatasia: diagnosis and clinical signs - a dental surgeon perspective.Genetic evaluations of Chinese patients with odontohypophosphatasia resulting from heterozygosity for mutations in the tissue-non-specific alkaline phosphatase gene.Four Novel Mutations in the ALPL Gene in Chinese patients with Odonto, Childhood and Adult Hypophosphatasia.
P2860
Novel ALPL genetic alteration associated with an odontohypophosphatasia phenotype.
description
2013 nî lūn-bûn
@nan
2013 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Novel ALPL genetic alteration associated with an odontohypophosphatasia phenotype.
@ast
Novel ALPL genetic alteration associated with an odontohypophosphatasia phenotype.
@en
type
label
Novel ALPL genetic alteration associated with an odontohypophosphatasia phenotype.
@ast
Novel ALPL genetic alteration associated with an odontohypophosphatasia phenotype.
@en
prefLabel
Novel ALPL genetic alteration associated with an odontohypophosphatasia phenotype.
@ast
Novel ALPL genetic alteration associated with an odontohypophosphatasia phenotype.
@en
P2093
P2860
P50
P1433
P1476
Novel ALPL genetic alteration associated with an odontohypophosphatasia phenotype
@en
P2093
Ana Paula Oliveira Giorgetti
Brian L Foster
Enilson A Sallum
Mariana Martins Ribeiro
Martha J Somerman
Márcio Z Casati
Thaisângela L Rodrigues
P2860
P304
P356
10.1016/J.BONE.2013.06.010
P577
2013-06-19T00:00:00Z