Dominant-negative kinase domain mutations in...

Human Molecular Genetics 2016 / 02

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

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, Maxi
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Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/ddw064
Date:
February, 2016
File:
PDF, 763 KB
english, 2016
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