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Fig. 1 | BMC Medical Genomics

Fig. 1

From: Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness

Fig. 1

Pedigree information showing segregation of TMIE variants. A Pedigree of family 1. ( +): a ~ 10-kb deletion B Pedigree of family 2. ( +): c.122_125dup (p.Pro43fs) C Pedigree of family 3. ( +): c. 250 C > T; p.(Arg84Trp). The ( −) indicates the wild-type allele. The arrows show the affected individual who was selected for whole-exome sequencing. In these figures, white symbols signify unaffected; black symbols mean affected; squares are men; circles are females; parallel lines show consanguineous marriage

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BMC Medical Genomics

ISSN: 1755-8794

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