Identification of homozygous missense variant in SIX5 gene underlying recessive nonsyndromic hearing impairment

Hearing impairment (HI) is a heterogeneous condition that affects many individuals globally with different age groups. HI is a genetically and phenotypically heterogeneous disorder. Over the last several years, many genes/loci causing rare autosomal recessive and dominant forms of hearing impairment...

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Detalles Bibliográficos
Autores principales: Kakar, Mohib Ullah, Akram, Muhammad, Zubair Mehboob, Muhammad, Younus, Muhammad, Bilal, Muhammad, Waqas, Ahmed, Nazir, Amina, Shafi, Muhammad, Umair, Muhammad, Ahmad, Sajjad, Rafeeq, Misbahuddin M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9202841/
https://www.ncbi.nlm.nih.gov/pubmed/35709191
http://dx.doi.org/10.1371/journal.pone.0268078

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9202841/
https://www.ncbi.nlm.nih.gov/pubmed/35709191
http://dx.doi.org/10.1371/journal.pone.0268078

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