X-linked hypophosphatemia in Polish patients. 1. Mutations in the PHEX gene.
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Genetic diagnosis of X-linked dominant Hypophosphatemic Rickets in a cohort study: tubular reabsorption of phosphate and 1,25(OH)2D serum levels are associated with PHEX mutation type.Mutational survey of the PHEX gene in patients with X-linked hypophosphatemic rickets.PHEX gene mutations and genotype-phenotype analysis of Korean patients with hypophosphatemic rickets.
P2860
X-linked hypophosphatemia in Polish patients. 1. Mutations in the PHEX gene.
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2000 nî lūn-bûn
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2000 թուականի Յունուարին հրատարակուած գիտական յօդուած
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2000 թվականի հունվարին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年论文
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name
X-linked hypophosphatemia in Polish patients. 1. Mutations in the PHEX gene.
@ast
X-linked hypophosphatemia in Polish patients. 1. Mutations in the PHEX gene.
@en
type
label
X-linked hypophosphatemia in Polish patients. 1. Mutations in the PHEX gene.
@ast
X-linked hypophosphatemia in Polish patients. 1. Mutations in the PHEX gene.
@en
prefLabel
X-linked hypophosphatemia in Polish patients. 1. Mutations in the PHEX gene.
@ast
X-linked hypophosphatemia in Polish patients. 1. Mutations in the PHEX gene.
@en
P2093
P1476
X-linked hypophosphatemia in Polish patients. 1. Mutations in the PHEX gene
@en
P2093
Jurkiewicz D
Krajewska-Walasek M
Popowska E
Pronicka E
Rowinska E
P304
P50
P577
2000-01-01T00:00:00Z