Bharadwaj, T., Schrauwen, I., Acharya, A., Nouel‐Saied, L. M., Väisänen, M., Kraatari, M., Rahikkala, E., Jarvela, I., Kotimäki, J., & Leal, S. M. (2022). Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant. Molecular Genetics & Genomic Medicine, 10(3). Portico. https://doi.org/10.1002/mgg3.1866
Subjects:
Deafness
(MeSH)
Hearing Loss
(MeSH)
Molecular Basis of Rett Syndrome and Related Disorders
(OpenAlex Topic)
Cochlear Neuropathy and Hearing Loss Mechanisms
(OpenAlex Topic)
Molecular Mechanisms of Cardiac Development and Regeneration
(OpenAlex Topic)
Publication Type:
Article
Unique ID:
10.1002/mgg3.1866
PMID:
DOI:
Publication Date:
Data Source:
Scopus