1 | IMF1, IMF2, NOTCH3, PDGFRB |
Mutations in PDGFRB Cause Autosomal-Dominant Infantile Myofibromatosis. | |
Martignetti JA, Tian L, Li D, Ramirez MC, Camacho-Vanegas O, Camacho SC, Guo Y, Zand DJ, Bernstein AM, Masur SK, Kim CE, Otieno FG, Hou C, Abdel-Magid N, Tweddale B, Metry D, Fournet JC, Papp E, McPherson EW, Zabel C, Vaksmann G, Morisot C, Keating B, Sleiman PM, Cleveland JA, Everman DB, Zackai E, Hakonarson H. | |
Am J Hum Genet m J Hum Genet. 2013 May 22. doi:pii: S0002-9297(13)00211-5. 10.1016/j.ajhg.2013.04.024. [Epub ahead of print] 2013 | |
2 | IMF1, IMF2, NOTCH3, PDGFRB |
Mutations in PDGFRB and NOTCH3 are the first genetic causes identified for autosomal dominant infantile myofibromatosis. | |
Lee JW. | |
Clin Genet 84(4):340-1. doi: 10.1111/cge.12238. Epub 2013 Jul 31. No abstract available. 2013 | |