3 results for author:"DeLuca A.P." in Literature citations
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| Exome sequencing and analysis of induced pluripotent stem cells identify the cilia-related gene male germ cell-associated kinase (MAK) as a cause of retinitis pigmentosa. Tucker B.A., Scheetz T.E., Mullins R.F., DeLuca A.P., Hoffmann J.M., Johnston R.M., Jacobson S.G., Sheffield V.C., Stone E.M. Proc. Natl. Acad. Sci. U.S.A. 108:E569-E576(2011) · UniProtKB (1) · Mapped (3) |
| DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss. Hildebrand M.S., Morin M., Meyer N.C., Mayo F., Modamio-Hoybjor S., Mencia A., Olavarrieta L., Morales-Angulo C., Nishimura C.J., Workman H. et al. Hum. Mutat. 32:825-834(2011) · UniProtKB (1) |
| Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4). Zheng J., Miller K.K., Yang T., Hildebrand M.S., Shearer A.E., DeLuca A.P., Scheetz T.E., Drummond J., Scherer S.E., Legan P.K. et al. Proc. Natl. Acad. Sci. U.S.A. 108:4218-4223(2011) · UniProtKB (3) · Mapped (8) |