Literature DB >> 16703383

DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2.

Regie Lyn P Santos1, Muhammad Jawad Hassan, Shaheen Sikandar, Kwanghyuk Lee, Ghazanfar Ali, Protacio E Martin, Michael Angelo L Wambangco, Wasim Ahmad, Suzanne M Leal.   

Abstract

From a large collection of families with autosomal recessive non-syndromic hearing impairment (NSHI) from Pakistan, linkage has been established for two unrelated consanguineous families to 19p13.2. This new locus was assigned the name DFNB68. A 10 cM genome scan and additional fine mapping were carried out using microsatellite marker loci. Linkage was established for both families to DFNB68 with maximum multipoint LOD scores of 4.8 and 4.6. The overlap of the homozygous regions between the two families was bounded by D19S586 and D19S584, which limits the locus interval to 1.9 cM and contains 1.4 Mb. The genes CTL2, KEAP1 and CDKN2D were screened but were negative for functional sequence variants.

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Year:  2006        PMID: 16703383      PMCID: PMC2909094          DOI: 10.1007/s00439-006-0188-z

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  18 in total

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  12 in total

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7.  Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2.

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Review 9.  Identification of autosomal recessive nonsyndromic hearing impairment genes through the study of consanguineous and non-consanguineous families: past, present, and future.

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Journal:  Hum Genet       Date:  2021-07-22       Impact factor: 4.132

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