Genetic underpinnings explored: OPA1 deletion and complex phenotypes on chromosome 3q29

Wang, E. H.-H., Lin, P.-H., Wu, P.-L., Kang, E. Y.-C., Liu, L., Yeh, L.-K., Chen, K.-J., Hsiao, M.-C., & Wang, N.-K. (2024). Genetic underpinnings explored: OPA1 deletion and complex phenotypes on chromosome 3q29. BMC Medical Genomics, 17(1). https://doi.org/10.1186/s12920-024-01850-6
Authors:
Ethan Hung-Hsi Wang
Pei-Hsuan Lin
Pei-Liang Wu
Eugene Yu-Chuan Kang
Laura Liu
Lung-Kun Yeh
Kuan-Jen Chen
Meng-Chang Hsiao
Nan-Kai Wang
Affiliated Authors:
Ethan Hung-Hsi Wang
Pei-Hsuan Lin
Pei-Liang Wu
Eugene Yu-Chuan Kang
Nan-Kai Wang
Subjects:
Author Keywords:
autosomal dominant optic atrophy
brain aneurysm
exome sequencing
microarray
opa1
Publication Type:
Article
Unique ID:
10.1186/s12920-024-01850-6
PMID:
Publication Date:
Data Source:
PubMed

Record Created: