MCT8 mutation analysis and identification of the first female with Allan–Herndon–Dudley syndrome due to loss of MCT8 expression

✍ Scribed by Frints, Suzanna Gerarda Maria; Lenzner, Steffen; Bauters, Mareike; Jensen, Lars Riff; Van Esch, Hilde; des Portes, Vincent; Moog, Ute; Macville, Merryn Victor Erik; van Roozendaal, Kees; Schrander-Stumpel, Constance Theresia Rimbertha Maria

• Book ID: 109848919
• Publisher: Nature Publishing Group
• Year: 2008
• Tongue: English
• Weight: 244 KB
• Volume: 16
• Category: Article
• ISSN: 1018-4813
• DOI: 10.1038/ejhg.2008.66