Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families.

Transl Psychiatry · 2020 · PMC7026119 · PMID 32066727

Europe PMC DOI

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closest p

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The sentences

nominally significantno p-value reported

In the RareIBD association analysis, two variants showed a nominally significant association with disease status: (i) variant p.N4041Y in the PKHD1L1 gene ( p nom = 0.0305); and (ii) variant p.R923Q in DCAF5 (family 0009, p nom = 0.0097).

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