Bi-Allelic MARVELD2 Variant Identified with Exome Sequencing in a Consanguineous Multiplex Ghanaian Family Segregating Non-Syndromic Hearing Loss

Twumasi Aboagye, E., Adadey, S. M., Alves de Souza Rios, L., Esoh, K. K., Wonkam-Tingang, E., Xhakaza, L., De Kock, C., Schrauwen, I., Amenga-Etego, L., Lang, D., Awandare, G. A., Leal, S. M., Mowla, S., & Wonkam, A. (2025). Bi-Allelic MARVELD2 Variant Identified with Exome Sequencing in a Consanguineous Multiplex Ghanaian Family Segregating Non-Syndromic Hearing Loss. International Journal of Molecular Sciences, 26(7), 3337. https://doi.org/10.3390/ijms26073337
Authors:
Elvis Twumasi Aboagye
Samuel Mawuli Adadey
Leonardo Alves de Souza Rios
Kevin K Esoh
Edmond Wonkam-Tingang
Lettilia Xhakaza
Carmen De Kock
Isabelle Schrauwen
Lucas Amenga-Etego
Dirk Lang
Gordon A Awandare
Suzanne M Leal
Shaheen Mowla
Ambroise Wonkam
Affiliated Authors:
Suzanne M Leal
Author Keywords:
non-syndromic hearing loss
marveld2
consanguinity
whole-exome sequencing
ghana
africa
Publication Type:
Article
Unique ID:
10.3390/ijms26073337
PMID:
Publication Date:
Data Source:
PubMed

Record Created: