Study of complex structural variations of X-linked deafness-2 based on single-molecule sequencing

X-linked deafness-2 (DFNX2) is cochlear incomplete partition type III (IP-III), one of inner ear malformations characterized by an abnormally wide opening in the bone separating the basal turn of the cochlea from the internal auditory canal, fixation of the stapes and cerebrospinal fluid (CSF) gushe...

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Detalles Bibliográficos
Autores principales: Jiang, Yi, Wu, Lihua, Huang, Shasha, Li, Pidong, Gao, Bo, Yuan, Yongyi, Zhang, Siwen, Yu, Guoliang, Gao, Yong, Wu, Hao, Dai, Pu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2021
Materias:
DNA, Chromosomes & Chromosomal Structure
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8193640/
https://www.ncbi.nlm.nih.gov/pubmed/33860785
http://dx.doi.org/10.1042/BSR20203740

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