1. Novel SBF1 splice‐site null mutation broadens the clinical spectrum of Charcot‐Marie‐Tooth type 4B3 disease. Issue 5 (9th August 2018) Authors: Flusser, H.; Halperin, D.; Kadir, R.; Shorer, Z.; Shelef, I.; Birk, O.S. Journal: Clinical genetics Issue: Volume 94:Issue 5(2018) Page Start: 473 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗