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. 2001 Jun;85(6):758-9.
doi: 10.1136/bjo.85.6.754d.

A new pedigree with recessive mapping to CHED2 locus on 20p13

M D Mohamed, M McKibbin, H Jafri, Y Rasheed, C G Woods, C F Inglehearn

A new pedigree with recessive mapping to CHED2 locus on 20p13

M D Mohamed et al. Br J Ophthalmol. 2001 Jun.
No abstract available

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Figures

Figure 1
Figure 1
Autosomal recessive CHED pedigree. Solid symbols show affected individuals and open symbols denote unaffected individuals, the spot indicates carrier status. Double marriage lines indicate a consanguineous pairing. The autosomal recessive and autosomal dominant CHED disease gene haplotypes are indicated, with allele fragment sizes shown for each genetic marker.
Figure 2
Figure 2
Opacified "ground glass" corneal appearance.
See this image and copyright information in PMC