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Q36919636-68950740-F1ED-4367-9FA4-E288DD6B2231
Q36919636-68950740-F1ED-4367-9FA4-E288DD6B2231
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36919636-68950740-F1ED-4367-9FA4-E288DD6B2231
Multiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRAS
P2860
Q36919636-68950740-F1ED-4367-9FA4-E288DD6B2231
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36919636-68950740-F1ED-4367-9FA4-E288DD6B2231
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wasDerivedFrom
7f74862e8eef25d126d12e018336932554d503d3
P2860
Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal development.