A novel SLC12A1 mutation in Bedouin kindred with antenatal Bartter syndrome type I-Reference-Cited by-同舟云学术

A novel SLC12A1 mutation in Bedouin kindred with antenatal Bartter syndrome type I

Published:2019-04-12 Issue:5 Volume:83 Page:361-366
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:Annals of Human Genetics

Author:

Halperin Daniel¹^ORCID,Dolgin Vadim¹,Geylis Michael²,Drabkin Max¹,Yogev Yuval¹,Wormser Ohad¹,Schreiber Ruth²,Shalev Hanna²,Landau Daniel³⁴,Birk Ohad S.¹⁵

Affiliation:

1. The Morris Kahn Laboratory of Human Genetics, National Institute for Biotechnology in the Negev and Faculty of Health Sciences Ben‐Gurion University of the Negev Beer‐Sheva Israel

2. Pediatric Nephrology Clinic, Soroka University Medical Center and Faculty of Health Sciences Ben‐Gurion University of the Negev Beer Sheva Israel

3. Pediatrics Department A, Soroka University Medical Center and Faculty of Health Sciences Ben‐Gurion University of the Negev Beer Sheva Israel

4. Pediatrics Department B Schneider Children's Medical Center Petah Tikva Israel

5. Genetics Institute, Soroka University Medical Center Ben‐Gurion University of the Negev Beer‐Sheva Israel

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ahg.12317

Reference19 articles.

1. Bartter syndrome: an overview

2. Phenotypic variability in Bartter syndrome type I

3. Antenatal Bartter Syndrome: A Review

4. Antenatal Bartter's syndrome: why is this not a lethal condition?

5. Secondary Nephrogenic Diabetes Insipidus as a Complication of Inherited Renal Diseases

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