Zobrazeno 1 - 1
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pro vyhledávání: '"Kübra Tekkuş Ermiş"'
Autor:
Nilüfer Göknar, Melda Ekici Avcı, Diana Üçkardeş, Emre Keleşoğlu, Kübra Tekkuş Ermiş, Cengiz Candan
Publikováno v:
Medeniyet Medical Journal
Medeniyet Medical Journal, Vol 36, Iss 4, Pp 352-355 (2021)
Medeniyet Medical Journal, Vol 36, Iss 4, Pp 352-355 (2021)
Mutations in hepatocyte nuclear factor-1 beta (HNF1B) are the most commonly identified genetic cause of renal malformations. Heterozygous mutations are associated with renal cysts and diabetes syndrome. Various renal developmental abnormalities and m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f2b4af3d439adbb8e25f11d7256c01d
http://europepmc.org/articles/PMC8694168
http://europepmc.org/articles/PMC8694168
