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Figure 1 | BMC Medical Genetics

Figure 1

From: Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan

Figure 1

Pedigree of Newfoundland family. There are ten hearing impaired individuals in a six generation extended family structure. Drawn below the enrolled subjects is a haplotype for STR markers around the DFNB8/B10 locus on chromosome 21. The carrier status of each person for the mutant alleles of TMPRSS3 found in this family is shown. "C" represents 207delC, while "T" stands for IVS8+8insT. Individuals V:17 and V:20 are compound heterozygotes.

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BMC Medical Genetics

ISSN: 1471-2350

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