GPSM2 and Chudley-McCullough Syndrome: A Dutch Founder Variant Brought to North America

Almomani, R.; Sun, Y.; Aten, E.; Hilhorst-Hofstee, Y.; Peeters-Scholte, C.M.P.C.D.; Haeringen, A. van; ... ; Santen, G.W.E. (2013)

Article / Letter to editor

• syndromic hearing loss
• GPSM2
• exome sequencing
• Chudley-McCullough syndrome

• All authors: Almomani, R.; Sun, Y.; Aten, E.; Hilhorst-Hofstee, Y.; Peeters-Scholte, C.M.P.C.D.; Haeringen, A. van; Hendriks, Y.M.C.; Dunnen, J.T. den; Breuning, M.H.; Kriek, M.; Santen, G.W.E.
• Date: 2013-05-31
• Journal: American Journal of Medical Genetics Part A
• Volume: 161A
• Issue: 5
• Pages: 973 - 976
• DOI: doi:10.1002/ajmg.a.35808