1. FC035: Exome Sequencing of the Israeli Dialysis-Treated Pediatric Population Reveals Monogenic Etiology in ∼44% of Cases. (3rd May 2022) Authors: Kagan, Maayan; Ben Moshe, Yishay; Shlomovitz, Omer; Atias-Varon, Danit; Haskin, Orly; Ben-Shalom, Efrat; Magen, Daniella; Schreiber, Ruth; Volovelsky, Oded; Shasha-Lavsky, Hadas; Davidovits, Miriam; Borovitz, Yael; Mor, Nofar; Khavkin, Yulia; Tzvi Behr, Shimrit; Pollack, Shirley; Geylis, Michael;... Journal: Nephrology dialysis transplantation Issue: Volume 37(2022)Supplement 3 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Myelin-associated glycoprotein gene mutation causes Pelizaeus-Merzbacher disease-like disorder. (15th July 2015) Authors: Lossos, Alexander; Elazar, Nimrod; Lerer, Israela; Schueler-Furman, Ora; Fellig, Yakov; Glick, Benjamin; Zimmerman, Bat-El; Azulay, Haim; Dotan, Shlomo; Goldberg, Sharon; Gomori, John M.; Ponger, Penina; Newman, J. P.; Marreed, Hodaifah; Steck, Andreas J.; Schaeren-Wiemers, Nicole; Mor, Nofar; Ha... Journal: Brain Issue: Volume 138:Part 9(2015:Sep.) Page Start: 2521 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗