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Figure 8. Sites of human enamelin gene mutations identified in families with AI. Exons are indicated by numbered boxes, introns by a line. The numbers below each exon show the range of amino acids encoded by that exon. Lines indicate the location of defined mutation sites in the enamelin gene. An "X" indicates that the mutation created a stop codon. Mutations affecting splice junctions are indicated by "spl jctn".
Crit. Rev. Oral Biol. Med., Vol. 14, No. 6,
387-398 (2003)
DOI: 10.1177/154411130301400602
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