Information Journal Paper
APA:
Copy. (2020). Whole exome sequencing identifies a novel homozygous duplication mutation in the VPS13B gene in an Indian family with Cohen syndrome. JOURNAL OF MOLECULAR NEUROSCIENCE, 70(8), 1225-1228. SID. https://sid.ir/paper/1023939/en
Vancouver:
Copy. Whole exome sequencing identifies a novel homozygous duplication mutation in the VPS13B gene in an Indian family with Cohen syndrome. JOURNAL OF MOLECULAR NEUROSCIENCE[Internet]. 2020;70(8):1225-1228. Available from: https://sid.ir/paper/1023939/en
IEEE:
Copy, “Whole exome sequencing identifies a novel homozygous duplication mutation in the VPS13B gene in an Indian family with Cohen syndrome,” JOURNAL OF MOLECULAR NEUROSCIENCE, vol. 70, no. 8, pp. 1225–1228, 2020, [Online]. Available: https://sid.ir/paper/1023939/en