Sprouty loss of function mutations in the mouse results in defects characteristic of 22q11 deletion syndrome, which are exacerbated by Tbx1 haploinsufficiency

✍ Scribed by Subreena Simrick; Dorota Szumska; Jennifer Gardiner; Sagar Karun; Bernice Morrow; Shoumo Bhattacharya; Michiel A. Basson

• Book ID: 113955285
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 58 KB
• Volume: 356
• Category: Article
• ISSN: 0012-1606
• DOI: 10.1016/j.ydbio.2011.05.366