A monoallelic variant in EYA1 is associated with Branchio-Otic syndrome in a Malian family

Yalcouyé, A., Traoré, O., Diarra, S., Schrauwen, I., Esoh, K., Kadlubowska, M. K., Bharadwaj, T., Adadey, S. M., Kéita, M., Guinto, C. O., Leal, S. M., Landouré, G., & Wonkam, A. (2022). A monoallelic variant in EYA1 is associated with Branchio‐Otic syndrome in a Malian family. Molecular Genetics & Genomic Medicine, 10(7). Portico. https://doi.org/10.1002/mgg3.1995
Authors:
Abdoulaye Yalcouyé
Oumou Traoré
Salimata Diarra
Isabelle Schrauwen
Kevin Esoh
Magda Kamila Kadlubowska
Thashi Bharadwaj
Samuel Mawuli Adadey
Mohamed Kéita
Cheick O. Guinto
Suzanne M. Leal
Guida Landouré
Ambroise Wonkam
Affiliated Authors:
Isabelle Schrauwen
Magda Kamila Kadlubowska
Thashi Bharadwaj
Suzanne M. Leal
Columbia Affiliation:
Subjects:
Hearing Loss (MeSH)
Intracellular Signaling Peptides and Proteins (MeSH)
Nuclear Proteins (MeSH)
Protein Tyrosine Phosphatases (MeSH)
Author Keywords:
africa
branchio-otic syndrome
eya1
mali
syndromic hearing impairment
elink
Publication Type:
Article
Unique ID:
10.1002/mgg3.1995
PMID:
35698919
DOI:
10.1002/mgg3.1995
Journal:
Molecular Genetics and Genomic Medicine
Publication Date:
Data Source:
Scopus
Source Link:
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Record Created: