Case Report: Novel Compound Heterozygous Variants in TRIOBP Associated With Congenital Deafness in a Chinese Family

Autosomal recessive non-syndromic deafness-28 (DFNB28) is characterized by prelingual, profound sensorineural hearing loss (HL). The disease is related to variants of the TRIOBP gene. TRIO and F-actin binding protein (TRIOBP) plays crucial roles in modulating the assembly of the actin cytoskeleton a...

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Detalles Bibliográficos
Autores principales: Zhou, Cong, Xiao, Yuanyuan, Xie, Hanbing, Wang, Jing, Liu, Shanling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8635749/
https://www.ncbi.nlm.nih.gov/pubmed/34868251
http://dx.doi.org/10.3389/fgene.2021.766973

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8635749/
https://www.ncbi.nlm.nih.gov/pubmed/34868251
http://dx.doi.org/10.3389/fgene.2021.766973

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