NEDO human cDNA sequencing project focused on splicing variants.Wakamatsu A., Yamamoto J., Kimura K., Ishii S., Watanabe K., Sugiyama A., Murakawa K., Kaida T., Tsuchiya K.[...], Isogai T.Cited forNUCLEOTIDE SEQUENCETissueLiverCategorySequencesSourceUniProtKB unreviewed (TrEMBL)Submission Submitted to EMBL/GenBank/DDBJ databases (OCT-2007)Cited in399+
Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4.Guernsey D.L., Jiang H., Hussin J., Arnold M., Bouyakdan K., Perry S., Babineau-Sturk T., Beis J., Dumas N.[...], Samuels M.E.View abstractAnnotationCEP152 is a strong candidate for the causal gene underlying MCPH4 and may be an important gene in the evolution of human brain size.CategorySequencesSourceGeneRif: 22995PubMedEurope PMCAm. J. Hum. Genet. 87:40-51 (2010)Cited in1Mapped to3
A Japanese-specific allele in the GALNT11 gene.Yuasa I., Umetsu K., Matsusue A., Nishimukai H., Harihara S., Fukumori Y., Saitou N., Jin F., Chattopadhyay P.K.[...], Henke J.View abstractAnnotationObservational study of genotype prevalence. (HuGE Navigator)CategorySequencesSourceGeneRif: 22995PubMedEurope PMCLeg. Med. 12:208-211 (2010)Cited in5Mapped to23