Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22–21.3

被引:0
|
作者
Muhammad Salman Chishti
Kwanghyuk Lee
Merry-Lynn McDonald
Muhammad Jawad Hassan
Muhammad Ansar
Wasim Ahmad
Suzanne M Leal
机构
[1] Quaid-I-Azam University,Department of Biochemistry
[2] Baylor College of Medicine,Department of Molecular and Human Genetics
来源
Journal of Human Genetics | 2009年 / 54卷
关键词
8p22–21.3; autosomal recessive non-syndromic hearing impairment; DFNB71; Pakistan;
D O I
暂无
中图分类号
学科分类号
摘要
A novel ARNSHI (autosomal recessive non-syndromic hearing impairment) locus, DFNB71, was localized to 8p22–21.3. To map the locus, a whole-genome scan was carried out using DNA samples from a consanguineous seven-generational Pakistani family with profound prelingual ARNSHI. A maximum multipoint LOD score of 4.2 occurred at marker D8S261. The DFNB71 region of homozygosity and 3-unit support interval is flanked by markers D8S1130 and D8S1786. This region has a genetic distance of 19.1 cM and contains 10.6 Mb of sequence.
引用
收藏
页码:141 / 144
页数:3
相关论文
共 50 条
  • [1] Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3
    Chishti, Muhammad Salman
    Lee, Kwanghyuk
    McDonald, Merry-Lynn
    Hassan, Muhammad Jawad
    Ansar, Muhammad
    Ahmad, Wasim
    Leal, Suzanne M.
    JOURNAL OF HUMAN GENETICS, 2009, 54 (03) : 141 - 144
  • [2] A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3
    Hassan, MJ
    Santos, RLP
    Rafiq, MA
    Chahrour, MH
    Pham, TL
    Wajid, M
    Hijab, N
    Wambangco, M
    Lee, K
    Ansar, M
    Yan, K
    Ahmad, W
    Leal, SM
    HUMAN GENETICS, 2006, 118 (05) : 605 - 610
  • [3] A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3
    Muhammad Jawad Hassan
    Regie Lyn P. Santos
    Muhammad Arshad Rafiq
    Maria H. Chahrour
    Thanh L. Pham
    Muhammad Wajid
    Nadine Hijab
    Michael Wambangco
    Kwanghyuk Lee
    Muhammad Ansar
    Kai Yan
    Wasim Ahmad
    Suzanne M. Leal
    Human Genetics, 2006, 118 : 605 - 610
  • [4] DFNB44, a novel autosomal recessive non-syndromic hearing impairment locus, maps to chromosome 7p14.1-q11.22
    Ansar, M
    Chahrour, MH
    Din, MAU
    Arshad, M
    Haque, S
    Pham, TL
    Yan, K
    Ahmad, W
    Leal, SM
    HUMAN HEREDITY, 2004, 57 (04) : 195 - 199
  • [5] The DFNB1 subtype of autosomal recessive non-syndromic hearing impairment
    del Castillo, Francisco J.
    del Castillo, Ignacio
    FRONTIERS IN BIOSCIENCE-LANDMARK, 2011, 16 : 3252 - 3274
  • [6] DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2
    Santos, Regie Lyn P.
    Hassan, Muhammad Jawad
    Sikandar, Shaheen
    Lee, Kwanghyuk
    Ali, Ghazanfar
    Martin, Protacio E., Jr.
    Wambangco, Michael Angelo L.
    Ahmad, Wasim
    Leal, Suzanne M.
    HUMAN GENETICS, 2006, 120 (01) : 85 - 92
  • [7] DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2
    Regie Lyn P. Santos
    Muhammad Jawad Hassan
    Shaheen Sikandar
    Kwanghyuk Lee
    Ghazanfar Ali
    Protacio E. Martin
    Michael Angelo L. Wambangco
    Wasim Ahmad
    Suzanne M. Leal
    Human Genetics, 2006, 120 : 85 - 92
  • [8] The mapping of DFNB62, a new locus for autosomal recessive non-syndromic hearing impairment, to chromosome 12p13.2-p11.23
    Ali, G
    Santos, RLP
    John, P
    Wambangco, MAL
    Lee, K
    Ahmad, W
    Leal, SM
    CLINICAL GENETICS, 2006, 69 (05) : 429 - 433
  • [9] DFNB86, a novel autosomal recessive non-syndromic deafness locus on chromosome 16p13.3
    Ali, R. A.
    Rehman, A. U.
    Khan, S. N.
    Husnain, T.
    Riazuddin, S.
    Friedman, T. B.
    Ahmed, Z. M.
    Riazuddin, S.
    CLINICAL GENETICS, 2012, 81 (05) : 498 - 500
  • [10] A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3
    Snoeckx, RL
    Kremer, H
    Ensink, RJH
    Flothmann, K
    de Brouwer, A
    Smith, RJH
    Cremers, CWRJ
    Van Camp, G
    JOURNAL OF MEDICAL GENETICS, 2004, 41 (01) : 11 - 13