An unusual case of hereditary nephrogenic diabetes insipidus (HNDI) affecting mother and daughter.

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An unusual case of hereditary nephrogenic diabetes insipidus (HNDI) affecting mother and daughter.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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An unusual case of hereditary ...... affecting mother and daughter.

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An unusual case of hereditary nephrogenic diabetes insipidus

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An unusual case of hereditary ...... affecting mother and daughter.

@en

An unusual case of hereditary nephrogenic diabetes insipidus

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An unusual case of hereditary ...... affecting mother and daughter.

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An unusual case of hereditary nephrogenic diabetes insipidus

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P1476

An unusual case of hereditary ...... affecting mother and daughter.

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P2093

Caroline Jones

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Dinesh Giri

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Ian Ellis

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Rachel Hart

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Renuka Ramakrishnan

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P2860

Cloning, characterization, and chromosomal mapping of human aquaporin of collecting duct

Central mechanisms of osmosensation and systemic osmoregulation

Molecular biology of hereditary diabetes insipidus.

Molecular and cellular defects in nephrogenic diabetes insipidus.

Nephrogenic diabetes insipidus: essential insights into the molecular background and potential therapies for treatment.

Diabetes insipidus--diagnosis and management.

Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutation.

Skewed X-chromosome inactivation causing diagnostic misinterpretation in congenital nephrogenic diabetes insipidus.

A novel deletion mutation in the arginine vasopressin receptor 2 gene and skewed X chromosome inactivation in a female patient with congenital nephrogenic diabetes insipidus.

Correlation between clinical phenotypes and X-inactivation patterns in six female carriers with heterozygote vasopressin type 2 receptor gene mutations.

P304

93-96

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scholarly article

P356

10.1515/JPEM-2015-0174

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P433

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P478

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P577

2016-01-01T00:00:00Z

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P698

26244674

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