3 results for author:"Erlich Y." in Literature citations
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| Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis. Erlich Y., Edvardson S., Hodges E., Zenvirt S., Thekkat P., Shaag A., Dor T., Hannon G.J., Elpeleg O. |
| Joubert syndrome 2 (JBTS2) in Ashkenazi Jews is associated with a TMEM216 mutation. Edvardson S., Shaag A., Zenvirt S., Erlich Y., Hannon G.J., Shanske A.L., Gomori J.M., Ekstein J., Elpeleg O. Am. J. Hum. Genet. 86:93-97(2010) · UniProtKB (1) |
| Hierarchical rules for Argonaute loading in Drosophila. Czech B., Zhou R., Erlich Y., Brennecke J., Binari R., Villalta C., Gordon A., Perrimon N., Hannon G.J. Mol. Cell 36:445-456(2009) · Mapped (40) |