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Ahsa1 and Hsp90 activity confers more severe craniofacial phenotypes in a zebrafish model of hypoparathyroidism, sensorineural deafness and renal dysplasia (HDR)

The severity of most human birth defects is highly variable. Our ability to diagnose, treat and prevent defects relies on our understanding of this variability. Mutation of the transcription factor GATA3 in humans causes the highly variable hypoparathyroidism, sensorineural deafness and renal dyspla...

詳細記述

保存先:
書誌詳細
主要な著者: Sheehan-Rooney, Kelly, Swartz, Mary E., Zhao, Feng, Liu, Dong, Eberhart, Johann K.
フォーマット: Artigo
言語:Inglês
出版事項: The Company of Biologists Limited 2013
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3759348/
https://ncbi.nlm.nih.gov/pubmed/23720234
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.011965
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