Search filters

A novel heterozygous deletion frameshift mutation of GATA3 in a Japanese kindred with the hypoparathyroidism, deafness and renal dysplasia syndrome.

Image Image of a generic work. The text above it indicates that there is no free image of the work available, and that if you own one, you can click on the placeholder link to upload it.
Description scientific article
Author/s

author: Hajime Yoshimura 

Publication date October 1, 2006
Language
Country of origin
Wikipedia link
Copyright status
Missing/wrong data? Edit Wikidata item