Citations for
1HOXA2, MCROT1
Identification of loss-of-function HOXA2 mutations in Chinese families with dominant bilateral microtia
Si N, Meng X, Lu X, Zhao X, Li C, Yang M, Zhang Y, Wang C, Guo P, Zhang X, Pan B, Jiang H.
Gene 2020 Oct 5;757:144945. doi: 10.1016/j.gene.2020.144945. Epub 2020 Jul 7. 2020
2HOXA2, MCROT1
Identification of a second HOXA2 nonsense mutation in a family with autosomal dominant non-syndromic microtia and distinctive ear morphology.
Piceci F, Morlino S, Castori M, Buffone E, De Luca A, Grammatico P, Guida V.
Clin Genet. May;91(5):774-779. doi: 10.1111/cge.12845. Epub 2016 Sep 13 2017
3HOXA2, MCROT1
HOXA2 haploinsufficiency in dominant bilateral microtia and hearing loss.
Brown KK, Viana LM, Helwig CC, Artunduaga MA, Quintanilla-Dieck L, Jarrin P, Osorno G, McDonough B, DePalma SR, Eavey RD, Seidman JG, Seidman CE.
Hum Mutat 34(10):1347-51. doi: 10.1002/humu.22367. Epub 2013 Jul 11. 2013
4MCROT1, HOXA2
A mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family.
Alasti F, Sadeghi A, Sanati MH, Farhadi M, Stollar E, Somers T, Van Camp G.
Am J Hum Genet 82(4):982-91. 2008