A Novel <i>ESRRB</i> Deletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment among Pakistani Families

<table>Pedigree drawing of family 4243. <i>Filled</i> symbols represent individuals with ARNSHI, and <i>clear</i> symbols represent hearing individuals. Displayed under each individual are the SNP markers within the region of the <i>ESRRB</i> gene and the p.Glu340del mutation.  The haplotype segregating with the ARNSHI phenotype is shown within a <i>box</i>. The homozygous region that is found only in ARNSHI individuals is bounded by rs917284 (chr14 : 71.8 Mb) and rs2043585 (chr14 : 79.0 Mb). The black arrow indicates the position of <i>ESRRB</i> gene amid the SNP marker loci.</table>

Genetics Research International

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Figure 1

Figure 1: A Novel <i>ESRRB</i> Deletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment among Pakistani Families 

Genetics Research International

A Novel ESRRB Deletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment among Pakistani Families

Figure 1