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A novel VPS13B mutation in two brothers with Cohen syndrome, cutis verticis gyrata and sensorineural deafness

✍ Scribed by Slim, Rima; Nürnberg, Gudrun; Ebermann, Inga; Nürnberg, Peter; Bolz, Hanno Jörn; Mégarbané, André

Book ID: 109848877
Publisher: Nature Publishing Group
Year: 2009
Tongue: English
Weight: 181 KB
Volume: 17
Category: Article
ISSN: 1018-4813
DOI: 10.1038/ejhg.2008.273

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