Human TBX1 Missense Mutations Cause Gain of Function Resulting in the Same Phenotype as 22q11.2 Deletions

✍ Scribed by Christiane Zweier; Heinrich Sticht; Inci Aydin-Yaylagül; Christine E. Campbell; Anita Rauch

• Book ID: 117854988
• Publisher: American Society of Human Genetics
• Year: 2007
• Tongue: English
• Weight: 477 KB
• Volume: 80
• Category: Article
• ISSN: 0002-9297
• DOI: 10.1086/511993