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

Author(s):: 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 (0000-0002-6304-1710); Breuning, M.H. (0000-0002-8212-4319); Kriek, M.; Santen, G.W.E.

Published: 2013
Publication type: Article / Letter to editor

syndromic hearing lossGPSM2exome sequencingChudley-McCullough syndrome

Date issued: 2013-05-31
Language: English
Is part of: American Journal of Medical Genetics Part A (2013), Vol. 161A, no. 5, p. 973-976
hdl: 1887/105210
doi: 10.1002/ajmg.a.35808