Localized Attachment Loss in Pendred Syndrome: Incidental? [PDF]
, 2007 Dileep Sharma, A.R. Pradeep
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Expression of Pendrin and the Pendred Syndrome (PDS) Gene in Human Thyroid Tissues* [PDF]
, 2000 Jean-Michel Bidart +6 more
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Measurements of endolymphatic K⁺ concentrations in the utricle of pre- and postnatal Slc26a4 Δ/+ and Slc26a4 Δ/Δ mice [PDF]
Master of ScienceDepartment of Anatomy and PhysiologyA. Philine WangemannSLC26A4 and its murine ortholog Slc26a4 code for pendrin, an anion-exchanger that is expressed in the inner ear.
Zhou, Fei
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Unilateral corneal anaesthesia and ulceration following squint surgery in a child with Pendred syndrome and bilateral sixth nerve palsy [PDF]
, 2003 Richard Wintle
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Genetic disorders in the Indian community of South Africa [PDF]
, 2016 OBJECTIVES: To determine the range of genetic disorders in the Indian population of South Africa, assess relevant historical and demographic factors, and discuss the implications for medical and genetic care.
Beighton, P, Winship, W S
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Mutations in the Pendred Syndrome (PDS/SLC26A) Gene: An Increasingly Complex Phenotypic Spectrum From Goiter to Thyroid Hypoplasia [PDF]
, 2014 Peter Kopp
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Strategies for genetic study of hearing loss in the \ud Brazilian northeastern region [PDF]
The overall aim of this study was to estimate the contribution of genetic factors to the etiology of hearing loss (HL) in two counties in the Brazilian northeastern region.
Andrade, Wagner T. +6 more
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Imaging profile of the ear in hearing loss patients in Hospital Universiti Sains Malaysia [PDF]
, 2015 Introduction: Hearing impairment is a major disability. The otologic assessments together with high-resolution CT images were able to obtain precise diagnostic profile of ear malformations.
Japar@Jaafar, Rohaizam
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Regulated acid-base transport in the collecting duct [PDF]
, 2018 The renal collecting system serves the fine-tuning of renal acid-base secretion. Acid-secretory type-A intercalated cells secrete protons via a luminally expressed V-type H+-ATPase and generate new bicarbonate released by basolateral chloride/bicarbonate
Bourgeois, Soline +3 more
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p.Y556C is a Recurrent Mutation in Pendred Syndrome causing Gene SLC26A4 in Punjabi Population [PDF]
, 2018 Sana Zahra
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