Complete androgen insensitivity syndrome caused by the R855H mutation in the androgen receptor gene.

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AR and SRD5A2 gene mutations in a series of 51 Turkish 46,XY DSD children with a clinical diagnosis of androgen insensitivity.

P2860

Q45151685-07971D66-6A95-47D5-BF58-44A105388DDA

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Complete androgen insensitivity syndrome caused by the R855H mutation in the androgen receptor gene.

Item

http://www.wikidata.org/entity/Q46424771

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2005 nî lūn-bûn

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

@zh-cn

2005年学术文章

@zh-hans

2005年学术文章

@zh-my

2005年学术文章

@zh-sg

2005年學術文章

@yue

2005年學術文章

@zh-hant

name

Complete androgen insensitivit ...... in the androgen receptor gene.

@en

Complete androgen insensitivit ...... in the androgen receptor gene.

@nl

type

Item

label

Complete androgen insensitivit ...... in the androgen receptor gene.

@en

Complete androgen insensitivit ...... in the androgen receptor gene.

@nl

prefLabel

Complete androgen insensitivit ...... in the androgen receptor gene.

@en

Complete androgen insensitivit ...... in the androgen receptor gene.

@nl

P1476

Complete androgen insensitivit ...... in the androgen receptor gene.

@en

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Carolina Sismani

http://www.w3.org/2001/XMLSchema#string

Charles Sultan

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Maria Perikleous

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Nicos Skordis

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Philippos C Patsalis

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Serge Lumbroso

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P2860

Studies of the locus for androgen receptor: localization on the human X chromosome and evidence for homology with the Tfm locus in the mouse

Assessment of the gonadotrophin-gonadal axis in androgen insensitivity syndrome

Phenotypic diversity in siblings with partial androgen insensitivity syndrome

Clinical, hormonal, behavioral, and genetic characteristics of androgen insensitivity syndrome in a Brazilian cohort: five novel mutations in the androgen receptor gene

Disorders linked to insufficient androgen action in male children

Genotype versus phenotype in families with androgen insensitivity syndrome

Clinical and biochemical investigations and molecular analysis of subjects with mutations in the androgen receptor gene

Longer polyglutamine tracts in the androgen receptor are associated with moderate to severe undermasculinized genitalia in XY males.

Disorders of androgen action.

Amino acid substitutions in the hormone-binding domain of the human androgen receptor alter the stability of the hormone receptor complex.

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309-313

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scholarly article

P356

10.1515/JPEM.2005.18.3.309

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2005-03-01T00:00:00Z

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P698

15813610

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P921

Complete androgen insensitivity syndrome

Complete androgen insensitivity syndrome caused by the R855H mutation in the androgen receptor gene.

about

P2860

P2860

Complete androgen insensitivity syndrome caused by the R855H mutation in the androgen receptor gene.

description

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type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921