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Detection of a multilineage mosaic NRAS mutation c.181C>A (p.Gln61Lys) in an individual with a complex congenital nevus syndrome
Author(s) -
Ulrich Maximilian,
Tinschert Sigrid,
Siebert Eberhard,
Franke Ingolf,
Tüting Thomas,
Ulrich Jens,
Schanze Denny,
Wieland Ilse,
Zenker Martin
Publication year - 2019
Publication title -
pigment cell and melanoma research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.618
H-Index - 105
eISSN - 1755-148X
pISSN - 1755-1471
DOI - 10.1111/pcmr.12761
Subject(s) - neuroblastoma ras viral oncogene homolog , mosaic , mutation , genetics , medicine , biology , gene , history , kras , archaeology