APA citiranje

Kinkar, J. S., Jameel, P. Z., Kumawat, B. L., & Kalbhor, P. (2021). Heterozygous deletion in exon 6 of STEX gene causing ataxia with oculomotor apraxia type 2 (AOA-2) with ovarian failure. BMJ Case Rep.

Citação norma Chicago

Kinkar, Jiwan Shriram, Patel Zeeshan Jameel, Banshi Lal Kumawat, and Priyanka Kalbhor. "Heterozygous Deletion in Exon 6 of STEX Gene Causing Ataxia With Oculomotor Apraxia Type 2 (AOA-2) With Ovarian Failure." BMJ Case Rep 2021.

MLA citiranje

Kinkar, Jiwan Shriram, Patel Zeeshan Jameel, Banshi Lal Kumawat, and Priyanka Kalbhor. "Heterozygous Deletion in Exon 6 of STEX Gene Causing Ataxia With Oculomotor Apraxia Type 2 (AOA-2) With Ovarian Failure." BMJ Case Rep 2021.