Germline Missense Mutations Affecting KRAS Isoform B Are Associated with a Severe Noonan Syndrome Phenotype

✍ Scribed by Claudio Carta; Francesca Pantaleoni; Gianfranco Bocchinfuso; Lorenzo Stella; Isabella Vasta; Anna Sarkozy; Cristina Digilio; Antonio Palleschi; Antonio Pizzuti; Paola Grammatico; Giuseppe Zampino; Bruno Dallapiccola; Bruce D. Gelb; Marco Tartaglia

• Book ID: 119770040
• Publisher: American Society of Human Genetics
• Year: 2006
• Tongue: English
• Weight: 895 KB
• Volume: 79
• Category: Article
• ISSN: 0002-9297
• DOI: 10.1086/504394