Mutation screening of the CYP1B1 gene reveals thirteen novel disease-causing variants in consanguineous Pakistani families causing primary congenital glaucoma.

Autor: Tehreem, Raeesa1 (AUTHOR), Arooj, Anam1 (AUTHOR), Siddiqui, Sorath Noorani2 (AUTHOR), Naz, Shagufta3 (AUTHOR), Afshan, Kiran1 (AUTHOR), Firasat, Sabika1 (AUTHOR) sabika.firasat@qau.edu.pk
Zdroj: PLoS ONE. 9/9/2022, Vol. 17 Issue 9, p1-15. 15p.
Databáze: Academic Search Ultimate
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