## Communicated by Dvorah Abeliovich In a consanguineous Turkish family, a locus for autosomal recessive nonsyndromic hearing impairment (ARNSHI) was mapped to chromosome 2q31.1-2q33.1. Microsatellite marker analysis in the complete family determined the critical linkage interval that overlapped w
β¦ LIBER β¦
Splice-site mutations in theTRICgene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families
β Scribed by Muhammad S. Chishti; Attya Bhatti; Sana Tamim; Kwanghyuk Lee; Merry-Lynn McDonald; Suzanne M. Leal; Wasim Ahmad
- Book ID
- 106252256
- Publisher
- Nature Publishing Group
- Year
- 2007
- Tongue
- English
- Weight
- 373 KB
- Volume
- 53
- Category
- Article
- ISSN
- 1435-232X
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Involvement of DFNB59 mutations in autos
β
Rob W.J. Collin; Ersan Kalay; Jaap Oostrik; Refik Γaylan; Bernd Wollnik; SelΓ§uk
π
Article
π
2007
π
John Wiley and Sons
π
English
β 311 KB
Mutations in the P2RY5 gene underlie aut
β
M. Tariq; M. Ayub; M. Jelani; S. Basit; G. Naz; N. Wasif; S.I. Raza; A.K. Naveed
π
Article
π
2009
π
John Wiley and Sons
π
English
β 544 KB
Novel sequence variants in theTMIEgene i
β
Regie Lyn P. Santos; Hatem El-Shanti; Shaheen Sikandar; Kwanghyuk Lee; Attya Bha
π
Article
π
2005
π
Springer
π
English
β 131 KB
A Novel Splice Site Mutation in the EDAR
β
NAVEED WASIF; MUHAMMAD TARIQ; GHAZANFAR ALI; MUHAMMAD JAWAD HASSAN; WASIM AHMAD
π
Article
π
2010
π
John Wiley and Sons
π
English
β 321 KB
Novel CLDN14 mutations in Pakistani fami
β
Kwanghyuk Lee; Muhammad Ansar; Paula B. Andrade; Bushra Khan; Regie Lyn P. Santo
π
Article
π
2012
π
John Wiley and Sons
π
English
β 293 KB
Novel sequence variants in the TMC1 gene
β
Regie Lyn P. Santos; Muhammad Wajid; Mohammad Nasim Khan; Nathan McArthur; Thanh
π
Article
π
2005
π
John Wiley and Sons
π
English
β 152 KB
Though many hearing impairment genes have been identified, only a few of these genes have been screened in population studies. For this study, 168 Pakistani families with autosomal recessive hearing impairment not due to mutations in the GJB2 (Cx26) gene underwent a genome scan. Two-point and multip