Rare variants in Protein tyrosine phosphatase, receptor type A (PTPRA) in schizophrenia: Evidence from a family based study

The contribution of both common and rare risk variants to the genetic architecture of schizophrenia (SZ) has been documented in genome-wide association studies, whole exome and whole genome sequencing approaches. As SZ is highly heritable and segregates in families, highly penetrant rare variants ar...

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Detaylı Bibliyografya
Yayımlandı:Schizophr Res
Asıl Yazarlar: John, Jibin, Kukshal, Prachi, Sharma, Aditya, Bhatia, Triptish, Nimgaonkar, V.L., Deshpande, S.N., Thelma, B.K.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2018
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7321970/
https://ncbi.nlm.nih.gov/pubmed/30594456
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.schres.2018.12.012
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