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Germline missense mutations affecting KRAS Isoform B are associated with a severe Noonan syndrome phenotype.
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
Am J Hum Genet 2006; 79(1):129-135
ICID: 841198
IC™ Value: 22.65
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  • Marco Tartaglia - click here