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SAT-065 A Novel De Novo GATA3 Gene Mutation in an Adolescent with HDR Syndrome

Background: GATA3 encodes a transcription factor critical for embryonic development of the parathyroid glands, kidney, inner ear, thymus, and the central nervous system. Heterozygous loss-of-function mutations in GATA3 are associated with hypoparathyroidism, sensorineural deafness and renal disease...

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Publicat a:J Endocr Soc
Autors principals: Cruz-Aviles, Lisa Michelle, Bale, Allen, Carpenter, Thomas O
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2020
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7208832/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.1845
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