| 1 | C12orf57, CLBMS1
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| Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia.
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| Akizu N, Shembesh NM, Ben-Omran T, Bastaki L, Al-Tawari A, Zaki MS, Koul R, Spencer E, Rosti RO, Scott E, Nickerson E, Gabriel S, da Gente G, Li J, Deardorff MA, Conlin LK, Horton MA, Zackai EH, Sherr EH, Gleeson JG.
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| Am J Hum Genet 92(3):392-400. doi: 10.1016/j.ajhg.2013.02.004. Epub 2013 Feb 28.
2013
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| 2 | C12orf57, CLBMS1
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| Mutations in c12orf57 cause a syndromic form of colobomatous microphthalmia.
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| Zahrani F, Aldahmesh MA, Alshammari MJ, Al-Hazzaa SA, Alkuraya FS.
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| Am J Hum Genet 92(3):387-91. doi: 10.1016/j.ajhg.2013.01.008. Epub 2013 Feb 28.
2013
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| 3 | C12orf57, EMG1, GPR162, LEPREL2, LPCAT3, PHB2, SPSB2
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| Large-scale sequencing in human chromosome 12p13: experimental and computational gene structure determination.
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| Ansari-Lari MA, Shen Y, Muzny DM, Lee W, Gibbs RA.
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| Genome Res 7(3):268-80. 1997
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| 4 | C12orf57, CD4, EMG1, GNB3, GPR162, LEPREL2, LPCAT3, PHB2, SPSB2, TPI1, USP5
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| A gene-rich cluster between the CD4 and triosephosphate isomerase genes at human chromosome 12p13.
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| Ansari-Lari MA, Muzny DM, Lu J, Lu F, Lilley CE, Spanos S, Malley T, GibbsRA.
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| Genome Res 6(4):314-26. 1996
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