Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population.

Autor: Naz, Arshi1 labarshi2013@gmail.com, Biswas, Arijit2,3, Nafees Khan, Tehmina1,4, Goodeve, Anne5,6, Ahmed, Nisar7, Saqlain, Nazish7, Ahmed, Shariq1,4, Ujjan, Ikram Din8, Shamsi, Tahir S.1,4, Oldenburg, Johannes2,9
Zdroj: Thrombosis Journal. 9/12/2017, Vol. 15, p1-8. 8p.
Databáze: Academic Search Ultimate