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Fig. 1 | BMC Medical Genomics

Fig. 1

From: Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15A

Fig. 1

Extended family pedigree, hearing phenotype and variant analysis. A Affected individuals are denoted in black. The arrow indicates the proband. The red dashed line indicates the two new affected individuals; B Audiogram of the two new affected individuals showing profound sensorineural hearing loss (red, right ear; blue, left ear); C Chromatogram of MYO15A (NM_016239.4): c.5531+1G > C and c.8375C > T in three affected individuals (II-2, II-3, III-1)

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BMC Medical Genomics

ISSN: 1755-8794

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