A TCTN2 mutation defines a novel Meckel Gruber syndrome locus.Shaheen R., Faqeih E., Seidahmed M.Z., Sunker A., Alali F.E., Alkuraya F.S.View abstractCited forTISSUE SPECIFICITY, DEVELOPMENTAL STAGECategoryExpressionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCHum. Mutat. 32:573-578 (2011)Cited in2
A high-resolution anatomical atlas of the transcriptome in the mouse embryo.Diez-Roux G., Banfi S., Sultan M., Geffers L., Anand S., Rozado D., Magen A., Canidio E., Pagani M.[...], Ballabio A.View abstractCategoryExpressionSourceMGI: 1915228PubMedEurope PMCPLoS Biol 9:e1000582-e1000582 (2011)Mapped to99+