Adadey, S. M., Aboagye, E. T., Esoh, K., Acharya, A., Bharadwaj, T., Lin, N. S., Amenga-Etego, L., Awandare, G. A., Schrauwen, I., Leal, S. M., & Wonkam, A. (2022). A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana. BMC Medical Genomics, 15(1). https://doi.org/10.1186/s12920-022-01391-w
Subjects:
Hearing Loss
(MeSH)
Cochlear Neuropathy and Hearing Loss Mechanisms
(OpenAlex Topic)
Impact of Hearing Loss on Cognitive Function
(OpenAlex Topic)
Molecular Mechanisms of Cardiac Development and Regeneration
(OpenAlex Topic)
Publication Type:
Article
Unique ID:
10.1186/s12920-022-01391-w
PMID:
Journal:
Publication Date:
Data Source:
Scopus