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Removal of an Internal Translational Start Site from mRNA While Retaining Expression of the Full-Length Protein
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A novel missense mutation in GJB2, p.Tyr65His, causes severe Vohwinkel syndrome

E A de Zwart-Storm1, M van Geel, E Veysey

  • 1Department of Dermatology, Maastricht University Medical Center, PO Box 5800, 6202 AZ Maastricht, The Netherlands. ea.de.zwart.storm@mumc.nl

The British Journal of Dermatology
|September 22, 2010
PubMed

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