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.

罕见的复合杂合错义 SPATA7 变异与精神分裂症风险；对近亲结婚家庭中患病兄弟姐妹进行全外显子组测序、后续测序和病例对照研究