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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Vydáno v:Schizophr Res
Hlavní autoři: John, Jibin, Kukshal, Prachi, Sharma, Aditya, Bhatia, Triptish, Nimgaonkar, V.L., Deshpande, S.N., Thelma, B.K.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2018
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On-line přístup: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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