Exome sequence analysis in consanguineous Pakistani families inheriting Bardet-Biedle syndrome determined founder effect of mutation c.299delC (p.Ser100Leufs*24) in BBS9 gene.

MLA

Muzammal, Muhammad, et al. “Exome Sequence Analysis in Consanguineous Pakistani Families Inheriting Bardet-Biedle Syndrome Determined Founder Effect of Mutation c.299delC (p.Ser100Leufs*24) in BBS9 Gene.” Molecular Genetics & Genomic Medicine, vol. 7, no. 8, Aug. 2019, p. e834. EBSCOhost, https://doi.org/10.1002/mgg3.834.

APA

Muzammal, M., Zubair, M., Bierbaumer, S., Blatterer, J., Graf, R., Gul, A., Abbas, S., Badar, M., Abbasi, A. A., Khan, M. A., & Windpassinger, C. (2019). Exome sequence analysis in consanguineous Pakistani families inheriting Bardet-Biedle syndrome determined founder effect of mutation c.299delC (p.Ser100Leufs*24) in BBS9 gene. Molecular Genetics & Genomic Medicine, 7(8), e834. https://doi.org/10.1002/mgg3.834

Chicago

Muzammal, Muhammad, Muhammad Zubair, Sophie Bierbaumer, Jasmin Blatterer, Ricarda Graf, Aisha Gul, Safdar Abbas, et al. 2019. “Exome Sequence Analysis in Consanguineous Pakistani Families Inheriting Bardet-Biedle Syndrome Determined Founder Effect of Mutation c.299delC (p.Ser100Leufs*24) in BBS9 Gene.” Molecular Genetics & Genomic Medicine 7 (8): e834. doi:10.1002/mgg3.834.