In a large kindred of German descent, we found a novel allele that segregates with deafness when present in trans with the 35delG allele of GJB2. Qualitative polymerase chain reaction–based allele-specific expression assays showed that expression of both GJB2 and GJB6 from the novel allele is dramatically reduced. This is the first evidence of a deafness-associated regulatory mutation of GJB2 and of potential coregulation of GJB2 and GJB6
AbstractObjectiveTo determine whether a new-born child from a family carrying a deafness gene needs ...
Fifty to eighty percent of autosomal recessive congenital severe to profound hearing impairment resu...
Mutations in the GJB2 gene (encoding for Connexin 26 protein) represent a leading cause of genetic h...
In a large kindred of German descent, we found a novel allele that segregates with deafness when pre...
Eleven affected members of a large German-American family segregating recessively inherited, congeni...
Eleven affected members of a large German\u2013American family segregating recessively inherited, co...
Mutations in the GJB2 gene, which encodes connexin 26, are a frequent cause of congenital non-syndro...
Single nucleotide polymorphisms (SNPs) are important markers in many studies that link DNA sequence ...
DFNB1 deafness, caused by mutations in the gene encoding connexin-26 (GJB2), is the most frequent su...
In many world populations, mutations in the GJB2 gene (codifyng for Connexin 26) are the most common...
Mutations in the GJB2 gene, which encodes connexin 26, are a frequent cause of congenital non-syndro...
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Single nucleotide polymorphisms ...
Previous studies of the gap-junction β-2 subunit gene GJB2 (connexin 26) have suggested that the 101...
GJB2 mutation analysis was performed in 179 unrelated subjects with sporadic or familial hearing los...
The DFNB1 subtype of autosomal recessive, nonsyndromic hearing impairment, caused by mutations affec...
AbstractObjectiveTo determine whether a new-born child from a family carrying a deafness gene needs ...
Fifty to eighty percent of autosomal recessive congenital severe to profound hearing impairment resu...
Mutations in the GJB2 gene (encoding for Connexin 26 protein) represent a leading cause of genetic h...
In a large kindred of German descent, we found a novel allele that segregates with deafness when pre...
Eleven affected members of a large German-American family segregating recessively inherited, congeni...
Eleven affected members of a large German\u2013American family segregating recessively inherited, co...
Mutations in the GJB2 gene, which encodes connexin 26, are a frequent cause of congenital non-syndro...
Single nucleotide polymorphisms (SNPs) are important markers in many studies that link DNA sequence ...
DFNB1 deafness, caused by mutations in the gene encoding connexin-26 (GJB2), is the most frequent su...
In many world populations, mutations in the GJB2 gene (codifyng for Connexin 26) are the most common...
Mutations in the GJB2 gene, which encodes connexin 26, are a frequent cause of congenital non-syndro...
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Single nucleotide polymorphisms ...
Previous studies of the gap-junction β-2 subunit gene GJB2 (connexin 26) have suggested that the 101...
GJB2 mutation analysis was performed in 179 unrelated subjects with sporadic or familial hearing los...
The DFNB1 subtype of autosomal recessive, nonsyndromic hearing impairment, caused by mutations affec...
AbstractObjectiveTo determine whether a new-born child from a family carrying a deafness gene needs ...
Fifty to eighty percent of autosomal recessive congenital severe to profound hearing impairment resu...
Mutations in the GJB2 gene (encoding for Connexin 26 protein) represent a leading cause of genetic h...