The Pendred syndrome gene encodes a chloride-iodide transport protein

Overview of attention for article published in Nature Genetics, April 1999

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So far, Altmetric has seen 4 citations on 4 Wikipedia pages.

English

Pendred syndrome

Cited by user CV9933 on 22 Jan 2021

Pendred syndrome is a genetic disorder leading to congenital bilateral (both sides) sensorineural hearing loss and goitre with euthyroid or mild hypothyroidism (decreased…

Ukrainian

SLC26A4

Cited by user SergoBot on 07 Sep 2017

French

Pendrine

Cited by user Bob Saint Clar on 28 Apr 2013

English

Pendrin

Cited by user Boghog on 26 Jul 2008

Pendrin, also known as sodium-independent chloride/iodide transporter, is a protein that in humans is encoded by the SLC26A4 gene (solute carrier family 26, member 4).

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