Newly discovered mutations in the GALNT3 gene causing autosomal recessive hyperostosis-hyperphosphatemia syndrome
about
A mouse with an N-Ethyl-N-nitrosourea (ENU) Induced Trp589Arg Galnt3 mutation represents a model for hyperphosphataemic familial tumoural calcinosisLong-term clinical outcome and phenotypic variability in hyperphosphatemic familial tumoral calcinosis and hyperphosphatemic hyperostosis syndrome caused by a novel GALNT3 mutation; case report and review of the literature.Familial tumoral calcinosis: from characterization of a rare phenotype to the pathogenesis of ectopic calcificationDisorders of phosphorus homeostasis.Rickets: Part II.EFEMP2 Mediates GALNT14-Dependent Breast Cancer Cell Invasion.
P2860
Newly discovered mutations in the GALNT3 gene causing autosomal recessive hyperostosis-hyperphosphatemia syndrome
description
2009 nî lūn-bûn
@nan
2009 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Newly discovered mutations in ...... sis-hyperphosphatemia syndrome
@ast
Newly discovered mutations in ...... sis-hyperphosphatemia syndrome
@en
type
label
Newly discovered mutations in ...... sis-hyperphosphatemia syndrome
@ast
Newly discovered mutations in ...... sis-hyperphosphatemia syndrome
@en
prefLabel
Newly discovered mutations in ...... sis-hyperphosphatemia syndrome
@ast
Newly discovered mutations in ...... sis-hyperphosphatemia syndrome
@en
P2093
P2860
P1433
P1476
Newly discovered mutations in ...... sis-hyperphosphatemia syndrome
@en
P2093
Eli Sprecher
Faysal Gok
Ilana Chefetz
Margarita Indelman
Murat Kocaoglu
P2860
P304
P356
10.1080/17453670902807482
P577
2009-02-01T00:00:00Z