RGD Annotation Report for Abnormal myelinationRat Genome Database

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An association has been curated linking KCNB1 and Abnormal myelination in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for human HPO-to-gene-to-disease annotations
697 RGD objects have been annotated to Abnormal myelination (HP:0012447)
11 papers in RGD have been used to annotate KCNB1
Original References(s): ORPHA:442835

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.