A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family

Manyisa, N., Schrauwen, I., de Souza Rios, L. A., Mowla, S., Tekendo-Ngongang, C., Popel, K., Esoh, K., Bharadwaj, T., Nouel-Saied, L. M., Acharya, A., Nasir, A., Wonkam-Tingang, E., Kock, C. de, Dandara, C., Leal, S. M., & Wonkam, A. (2021). A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family. Genes, 12(11), 1765. https://doi.org/10.3390/genes12111765
Authors:
Noluthando Manyisa
Isabelle Schrauwen
Leonardo Alves de Souza Rios
Shaheen Mowla
Cedrik Tekendo-Ngongang
Kalinka Popel
Kevin Esoh
Thashi Bharadwaj
Liz M Nouel-Saied
Anushree Acharya
Abdul Nasir
Edmond Wonkam-Tingang
Carmen de Kock
Collet Dandara
Suzanne M Leal
Ambroise Wonkam
Affiliated Authors:
Isabelle Schrauwen
Thashi Bharadwaj
Liz M Nouel-Saied
Anushree Acharya
Suzanne M Leal
Columbia Affiliation:
Subjects:
Cochlear Neuropathy and Hearing Loss Mechanisms (OpenAlex Topic)
Notch Signaling Pathway in Development and Disease (OpenAlex Topic)
Role of Long Noncoding RNAs in Cancer and Development (OpenAlex Topic)
Amino Acid Substitution (MeSH)
Exome Sequencing (MeSH)
Hearing Loss, Sensorineural (MeSH)
Neoplasm Proteins (MeSH)
Proto-Oncogene Proteins (MeSH)
Repressor Proteins (MeSH)
Author Keywords:
rest
re1-silencing transcription factor
non-syndromic hearing impairment
south africa
africa
dfna27
elink
Publication Type:
Article
Unique ID:
10.3390/genes12111765
PMID:
34828371
DOI:
10.3390/genes12111765
Journal:
Genes
Publication Date:
Data Source:
PubMed
Source Link:
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Record Created: