A novel HSF4 gene mutation (p.R405X) causing autosomal recessive congenital cataracts in a large consanguineous family from Pakistan.

BMC Med Genet · 2008 · PMC2592245 · PMID 19014451

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highly significantno p-value reported

A highly significant maximum two-point LOD score was obtained at D16S421 (Zmax = 5.6 at θ = 0) (table 1 ).

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