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