Nature

Genome-wide analysis reveals a novel autosomal-recessive hearing loss locus DFNB80 on chromosome 2p16.1-p21

Hearing impairment (HI) is the decreased ability to hear and discriminate among sounds. It is one of the most common birth defects. Epidemiological data show that more than one child in 1000 is born ...
Nature

Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort

Autosomal recessive nonsyndromic deafness (ARNSD) is characterized by a high degree of genetic heterogeneity, with reported mutations in 58 different genes. This study was designed to detect ...
Mena FN

Autosomal Dominant Optic Atrophy Market Set For Steady Growth Through 2034 As Gene And RNA-Based Therapies Advance Through Clinical Trials Delveinsight

"Autosomal Dominant Optic Atrophy Market Insight, Epidemiology And Market Forecast - 2034"The autosomal dominant optic atrophy (ADOA) treatment market is experiencing steady expansion, driven by ...