APA
Ivanov I. S., Azmanov D. N., Ivanova M. B., Chamova T., Pacheva I. H., Panova M. V., Song S., Morar B., Yordanova R. V., Galabova F. K., Sotkova I. G., Linev A. J., Bitchev S., Shearwood A. J., Kancheva D., Gabrikova D., Karcagi V., Guergueltcheva V., Geneva I. E., Bozhinova V., Stoyanova V. K., Kremensky I., Jordanova A., Savov A., Horvath R., Brown M. A., Tournev I., Filipovska A. & Kalaydjieva L. (20150610). Founder p.Arg 446* mutation in the PDHX gene explains over half of cases with congenital lactic acidosis in Roma children. : Molecular genetics and metabolism.
Chicago
Ivanov Ivan S, Azmanov Dimitar N, Ivanova Mariya B, Chamova Teodora, Pacheva Ilyana H, Panova Margarita V, Song Sharon, Morar Bharti, Yordanova Ralitsa V, Galabova Fani K, Sotkova Iglika G, Linev Alexandar J, Bitchev Stoyan, Shearwood Anne-Marie J, Kancheva Dalia, Gabrikova Dana, Karcagi Veronika, Guergueltcheva Velina, Geneva Ina E, Bozhinova Veneta, Stoyanova Vili K, Kremensky Ivo, Jordanova Albena, Savov Aleksey, Horvath Rita, Brown Matthew A, Tournev Ivailo, Filipovska Aleksandra and Kalaydjieva Luba. 20150610. Founder p.Arg 446* mutation in the PDHX gene explains over half of cases with congenital lactic acidosis in Roma children. : Molecular genetics and metabolism.
Harvard
Ivanov I. S., Azmanov D. N., Ivanova M. B., Chamova T., Pacheva I. H., Panova M. V., Song S., Morar B., Yordanova R. V., Galabova F. K., Sotkova I. G., Linev A. J., Bitchev S., Shearwood A. J., Kancheva D., Gabrikova D., Karcagi V., Guergueltcheva V., Geneva I. E., Bozhinova V., Stoyanova V. K., Kremensky I., Jordanova A., Savov A., Horvath R., Brown M. A., Tournev I., Filipovska A. and Kalaydjieva L. (20150610). Founder p.Arg 446* mutation in the PDHX gene explains over half of cases with congenital lactic acidosis in Roma children. : Molecular genetics and metabolism.
MLA
Ivanov Ivan S, Azmanov Dimitar N, Ivanova Mariya B, Chamova Teodora, Pacheva Ilyana H, Panova Margarita V, Song Sharon, Morar Bharti, Yordanova Ralitsa V, Galabova Fani K, Sotkova Iglika G, Linev Alexandar J, Bitchev Stoyan, Shearwood Anne-Marie J, Kancheva Dalia, Gabrikova Dana, Karcagi Veronika, Guergueltcheva Velina, Geneva Ina E, Bozhinova Veneta, Stoyanova Vili K, Kremensky Ivo, Jordanova Albena, Savov Aleksey, Horvath Rita, Brown Matthew A, Tournev Ivailo, Filipovska Aleksandra and Kalaydjieva Luba. Founder p.Arg 446* mutation in the PDHX gene explains over half of cases with congenital lactic acidosis in Roma children. : Molecular genetics and metabolism. 20150610.