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Linkage mapping of Thiel-Behnke corneal dystrophy (CDB2) to chromosome 10q23-q24.
Genomics. 1997 Nov 15;46(1):152-4. doi: 10.1006/geno.1997.5028.
Genomics. 1997.
PMID: 9403072
A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy.
Sullivan LS, Baylin EB, Font R, Daiger SP, Pepose JS, Clinch TE, Nakamura H, Zhao XC, Yee RW.
Sullivan LS, et al.
Mol Vis. 2007 Jun 21;13:975-80.
Mol Vis. 2007.
PMID: 17653038
Free PMC article.
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