Dominant-negative kinase domain mutations in FGFR1 can explain the clinical severity of Hartsfield syndrome

Por Hong, Sungkook, Hu, Ping, Marino, Juliana, Hufnagel, Sophia B., Hopkin, Robert J., Toromanović, Alma, Richieri-Costa, Antonio, Ribeiro-Bicudo, Lucilene A., Kruszka, Paul, Roessler, Erich, Muenke, Maximilian
Publicado no Hum Mol Genet (2016)