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Germline mutation in BRAF codon 600 is compatible with human development: de novo p.V600G mutation identified in a patient with CFC syndrome.
Champion, K J; Bunag, C; Estep, A L; Jones, J R; Bolt, C H; Rogers, R C; Rauen, K A; Everman, D B.
Affiliation
  • Champion KJ; Greenwood Genetic Center, Greenwood, SC 29646, USA.
Clin Genet ; 79(5): 468-74, 2011 May.
Article in En | MEDLINE | ID: mdl-20735442
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Codon / Germ-Line Mutation / Proto-Oncogene Proteins B-raf Type of study: Prognostic_studies Limits: Adult / Child, preschool / Female / Humans / Male Language: En Journal: Clin Genet Year: 2011 Document type: Article Affiliation country: United States Country of publication: Denmark
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Codon / Germ-Line Mutation / Proto-Oncogene Proteins B-raf Type of study: Prognostic_studies Limits: Adult / Child, preschool / Female / Humans / Male Language: En Journal: Clin Genet Year: 2011 Document type: Article Affiliation country: United States Country of publication: Denmark