Germline missense mutations affecting KRAS Isoform B are associated with a severe Noonan syndrome phenotype by Carta Claudio, Pantaleoni Francesca, Bocchinfuso Gianfranco, Stella Lorenzo, Vasta Isabella, Sarkozy Anna, Digilio Cristina, Palleschi Antonio, Pizzuti Antonio, Grammatico Paola, Zampino Giuseppe, Dallapiccola Bruno, Gelb Bruce D, Tartaglia Marco in American journal of human genetics (2006).

[PMID: 16773572] PubMed

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