In silico analysis of mutation spectrum of Ehlers–Danlos, osteogenesis imperfecta, and cutis laxa overlapping phenotypes in Iranian population.

Autor: Khosravi, Teymoor1 (AUTHOR), Naghipoor, Karim1 (AUTHOR), Vaghefi, Fatemeh1 (AUTHOR), Falahati, Ali Mohammad1 (AUTHOR), Oladnabi, Morteza2,3,4 (AUTHOR) oladnabidozin@yahoo.com
Zdroj: Egyptian Journal of Medical Human Genetics. 1/23/2024, Vol. 25 Issue 1, p1-20. 20p.
Databáze: Academic Search Ultimate
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