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References

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    Xin B, Puffenberger EG, Turben S, Tan H, Zhou A, Wang H. Homozygous frameshift mutation in TMCO1 causes a syndrome with craniofacial dysmorphism, skeletal anomalies, and mental retardation. Proc Natl Acad Sci USA 2010: 107: 258263.
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    Bilguvar K, Ozturk AK, Louvi A et al. Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations. Nature 2010: 467: 207210.
  • 3
    Zhang Z, Mo D, Cong P et al. Molecular cloning, expression patterns and subcellular localization of porcine TMCO1 gene. Mol Biol Rep 2010: 37: 16111618.