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A novel locusDFNA59for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2–q12.3

✍ Scribed by Arunima Chatterjee; Rajeev Jalvi; Nishtha Pandey; R. Rangasayee; Anuranjan Anand


Publisher
Springer
Year
2008
Tongue
English
Weight
379 KB
Volume
124
Category
Article
ISSN
0340-6717

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A novel autosomal recessive nonsyndromic
✍ Muhammad Aslam; Muhammad Wajid; Maria H. Chahrour; Muhammad Ansar; Sayedul Haque 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 78 KB 👁 1 views

A consanguineous family with autosomal recessive nonsyndromic hearing impairment (NSHI) was ascertained in Pakistan and displayed significant evidence of linkage to 3q13.31-q22.3. The novel locus (DFNB42) segregating in this kindred, maps to a 21.6 cM region according to a genetic map constructed us