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Missense Variants in Human GRXCR1 Are Associated with Congenital Nonsyndromic Hearing Loss
(A and B) Consanguineous pedigrees, sequence chromatograms of probands (arrows), and partial alignments of GRXCR1 encoded by genomic sequences from probands and controls and from other vertebrate species are shown for the double homozygous variants p.G64S (c.190G>A) and p.F153V (c.457T>G) (A) and for the single variant p.P38L (c.113C>T) (B).
