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...

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Detalles Bibliográficos
Autores principales: Sheehan-Rooney, Kelly, Swartz, Mary E., Zhao, Feng, Liu, Dong, Eberhart, Johann K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Limited 2013
Materias:
Research Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759348/
https://www.ncbi.nlm.nih.gov/pubmed/23720234
http://dx.doi.org/10.1242/dmm.011965

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759348/
https://www.ncbi.nlm.nih.gov/pubmed/23720234
http://dx.doi.org/10.1242/dmm.011965

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