THBS1 is a new autosomal recessive non-syndromic hearing impairment gene
Work
Year: 2024
Type: article
Abstract: Prelingual hearing impairment (HI) is genetically highly heterogenous. Early diagnosis and intervention are essential for psychosocial development. In this study we investigated a consanguineous famil... more
Source: BMC Medical Genomics
Institutions Columbia University Irving Medical Center, Quaid-i-Azam University, Kohat University of Science and Technology, Shaheed Benazir Bhutto University, University of Arizona
Cites: 33
Cited by:
Related to: 10
FWCI:
Citation percentile (by year/subfield):
Subfield: Sensory Systems
Field: Neuroscience
Domain: Life Sciences
Open Access status: gold
APC paid (est): $2,195