APA Alıntı

Igeta, H., Watanabe, Y., Morikawa, R., Ikeda, M., Otsuka, I., Hoya, S., . . . Someya, T. (2019). Rare compound heterozygous missense SPATA7 variations and risk of schizophrenia; whole-exome sequencing in a consanguineous family with affected siblings, follow-up sequencing and a case-control study. Neuropsychiatr Dis Treat.

Chicago Stili Alıntı

Igeta, Hirofumi, et al. "Rare Compound Heterozygous Missense SPATA7 Variations and Risk of Schizophrenia; Whole-exome Sequencing in a Consanguineous Family With Affected Siblings, Follow-up Sequencing and a Case-control Study." Neuropsychiatr Dis Treat 2019.

MLA Alıntı

Igeta, Hirofumi, et al. "Rare Compound Heterozygous Missense SPATA7 Variations and Risk of Schizophrenia; Whole-exome Sequencing in a Consanguineous Family With Affected Siblings, Follow-up Sequencing and a Case-control Study." Neuropsychiatr Dis Treat 2019.

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