Ajmal, M., Mir, A., Wahid, S., Khor, C. C., Foo, J. N., Siddiqi, S., . . . Nasir, M. (2017). Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family. BMC Med Genet.
Παραπομπή Chicago StyleAjmal, Muhammad, Asif Mir, Sughra Wahid, Chiea Chuen Khor, Jia Nee Foo, Saima Siddiqi, Mehran Kauser, Salman Akbar Malik, και Muhammad Nasir. "Identification and in Silico Characterization of a Novel P.P208PfsX1 Mutation in V-ATPase A3 Subunit Associated With Autosomal Recessive Osteopetrosis in a Pakistani Family." BMC Med Genet 2017.
Παραπομπή MLAAjmal, Muhammad, et al. "Identification and in Silico Characterization of a Novel P.P208PfsX1 Mutation in V-ATPase A3 Subunit Associated With Autosomal Recessive Osteopetrosis in a Pakistani Family." BMC Med Genet 2017.