Identification of two novel mutations in the PHEX gene in Chinese patients with hypophosphatemic rickets/osteomalacia.
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Whole Exome Sequencing Reveals Novel PHEX Splice Site Mutations in Patients with Hypophosphatemic Rickets.Genetic Testing Confirmed the Early Diagnosis of X-Linked Hypophosphatemic Rickets in a 7-Month-Old InfantSeven novel and six de novo PHEX gene mutations in patients with hypophosphatemic rickets.CHD1 regulates cell fate determination by activation of differentiation-induced genes.
P2860
Identification of two novel mutations in the PHEX gene in Chinese patients with hypophosphatemic rickets/osteomalacia.
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2014 nî lūn-bûn
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2014 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի մայիսին հրատարակված գիտական հոդված
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2014年の論文
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2014年学术文章
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2014年学术文章
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2014年学术文章
@zh-hans
2014年学术文章
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2014年学术文章
@zh-sg
2014年學術文章
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name
Identification of two novel mu ...... phatemic rickets/osteomalacia.
@ast
Identification of two novel mu ...... phatemic rickets/osteomalacia.
@en
type
label
Identification of two novel mu ...... phatemic rickets/osteomalacia.
@ast
Identification of two novel mu ...... phatemic rickets/osteomalacia.
@en
prefLabel
Identification of two novel mu ...... phatemic rickets/osteomalacia.
@ast
Identification of two novel mu ...... phatemic rickets/osteomalacia.
@en
P2093
P2860
P1433
P1476
Identification of two novel mu ...... phatemic rickets/osteomalacia.
@en
P2093
Jie-mei Gu
Jin-wei He
Wei-wei Hu
Wen-zhen Fu
Yu-juan Liu
P2860
P304
P356
10.1371/JOURNAL.PONE.0097830
P407
P577
2014-05-16T00:00:00Z