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J.1399-0004.2010.01495.X
J.1399-0004.2010.01495.X
http://dx.doi.org/10.1111/J.1399-0004.2010.01495.X
Germline mutation in BRAF codon 600 is compatible with human development: de novo p.V600G mutation identified in a patient with CFC syndrome.
P356
Q44394416-74512861-6C10-479F-B3C2-DD595FB41E2F
P356
J.1399-0004.2010.01495.X
http://dx.doi.org/10.1111/J.1399-0004.2010.01495.X