1. Clinical utility gene card for: Gitelman syndrome
- Author
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Olivier Devuyst, Erik-Jan Kamsteeg, Nine V A M Knoers, UCL - SSS/IREC/NEFR - Pôle de Néphrologie, and UCL - (SLuc) Service de néphrologie
- Subjects
Receptors, Drug - genetics ,medicine.medical_specialty ,Chloride Channels/genetics ,Solute Carrier Family 12 ,Member 3 ,Receptors, Drug ,030232 urology & nephrology ,Biology ,Genomic disorders and inherited multi-system disorders [IGMD 3] ,03 medical and health sciences ,Gitelman Syndrome/genetics ,0302 clinical medicine ,Chloride Channels ,Internal medicine ,Receptors ,Genetics ,medicine ,Hum ,Humans ,Solute Carrier Family 12, Member 3 ,Gene ,Genetics (clinical) ,030304 developmental biology ,0303 health sciences ,Symporters/genetics ,Chloride Channels - genetics ,Symporters ,Gitelman syndrome ,medicine.disease ,Endocrinology ,Gitelman Syndrome - genetics ,Drug/genetics ,Mutation (genetic algorithm) ,Mutation ,Clinical Utility Gene Card ,Genetics and epigenetic pathways of disease Renal disorder [NCMLS 6] ,Symporters - genetics ,Gitelman Syndrome ,Receptors, Drug/genetics - Abstract
Knoers, Nine Vam Devuyst, Olivier Kamsteeg, Erik-Jan Research Support, Non-U.S. Gov't England Eur J Hum Genet. 2011 Aug;19(8). doi: 10.1038/ejhg.2011.14. Epub 2011 Feb 23.
- Published
- 2011