Advanced search

Authors whose works are in public domain in at least one jurisdiction

List of works by Tayyab Husnain

1-6 of 6 results

View this query on the Wikidata Query Service
Mutations of MYO6 are associated with recessive deafness, DFNB37

scientific article
Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74

scientific article
Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing.

scientific article
Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome.

scientific article published on 30 July 2009
Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2-q13.3.

scientific article
The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3.

scientific article published on 10 August 2007

Paulina is supported by:

About Paulina

Help