Zobrazeno 1 - 2
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pro vyhledávání: '"Jon DeWitte"'
Publikováno v:
F1000Research, Vol 6 (2017)
Background: Aniridia is a disorder predominately caused by heterozygous loss-of-function mutations of the PAX6 gene, which is a transcriptional regulator necessary for normal eye and brain development. The ocular abnormalities of aniridia have been w
Externí odkaz:
https://doaj.org/article/9c3e5357a6c1448b8dda58ceb7399b15
Publikováno v:
F1000Research
Background:Aniridia is a disorder predominately caused by heterozygous loss-of-function mutations of thePAX6gene, which is a transcriptional regulator necessary for normal eye and brain development. The ocular abnormalities of aniridia have been well
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21a78a22c1cd7fb5985cefae5a85792e
https://doi.org/10.12688/f1000research.11063.1
https://doi.org/10.12688/f1000research.11063.1