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Gene Review

AIH3  -  amelogenesis imperfecta 3, hypomaturation...

Homo sapiens

 
 
 
 
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High impact information on AIH3

  • Linkage analysis has shown that there is genetic hetetogeneity in X-linked amelogenesis imperfecta with two identified loci: AIH1 and AIH3 [1].
  • The AIH3 locus maps to the Xq24-q27.1 region on the long arm of the X chromosome [1].

References

  1. Molecular biology of hereditary enamel defects. Aldred, M.J., Crawford, P.J. Ciba Found. Symp. (1997) [Pubmed]
 
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