Localisation of Pseudohypoaldosteronism Genes to Chromosome 16p12.2–13.11 and 12p13.1-Pter by Homozygosity Mapping-Reference-Cited by-同舟云学术

Localisation of Pseudohypoaldosteronism Genes to Chromosome 16p12.2–13.11 and 12p13.1-Pter by Homozygosity Mapping

Published:1996-02 Issue:2 Volume:5 Page:293-299
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Strautnieks Sandra S.,Thompson Richard J.,Hanukoglu Aaron,Dillon Michael J.,Hanukoglu Israel,Kuhnle Ursula,Seckl Jonathan,Gardiner R. Mark,Chung Eddie

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/5/2/293/7904112/5-2-293.pdf

Reference34 articles.

1. A Salt Wasting Syndrome in Infancy

2. 6 Mineralocorticoid resistance

3. Type I Pseudohypoaldosteronism Includes Two Clinically and Genetically Distinct Entities with either Renal or Multiple Target Organ Defects

4. The enigma of pseudohypoaldosteronism

5. Pseudohypoaldosteronism in Eight Families: Different Forms of Inheritance Are Evidence for Various Genetic Defects

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