Segawa syndrome due to mutation Q89X in theGCH1gene: a possible founder effect in Córdoba (southern Spain)

✍ Scribed by Eduardo López-Laso; Juan José Ochoa-Sepúlveda; Juan José Ochoa-Amor; Enrique Bescansa-Heredero; Rafael Camino-León; Francisco Javier Gascón-Jiménez; Maria Elena Mateos-González; Juan Luis Pérez-Navero; José Ignacio Lao-Villadóniga; Aida Ormazabal; Rafael Artuch; Katrin Beyer

• Publisher: Springer
• Year: 2009
• Tongue: English
• Weight: 232 KB
• Volume: 256
• Category: Article
• ISSN: 0340-5354
• DOI: 10.1007/s00415-009-5198-z