Mitochondrial Deafness
Mitochondrial Deafness is a sensorineural hearing impairment resulting from pathogenic mutations in mitochondrial DNA or nuclear genes affecting mitochondrial function, distinguished by its matrilineal inheritance pattern and association with oxidative phosphorylation deficits in cochlear cells.
299
Publications
19.9K
Citations
1.7K
Authors
609
Institutions
Publications per year
2017–2026
36
Parents
299
Xavier Estivill, Nancy Govea, Anna Barceló et al. · The American Journal of Human Genetics · 1998 · 549 citations · Full text
Hui Zhao, Ronghua Li, Qiuju Wang et al. · The American Journal of Human Genetics · 2004 · 424 citations · Full text
1–5 of 299
1.7K
Cincinnati Children's Hospital Medical Center, United States
51 publications · 4K citations
35
h-index
18
h-index
Cincinnati Children's Hospital Medical Center, United States
13 publications · 1.1K citations
13
h-index
12
h-index
11
h-index
1–5 of 1.7K
609

Cincinnati Children's Hospital Medical Center
Cincinnati, United States
30 h-index
113 publications
10.9K citations

University of Cincinnati Medical Center
Cincinnati, United States
22 h-index
33 publications
2.5K citations
Wenzhou Medical University
Wenzhou, China
19 h-index
147 publications
10.3K citations

Zhejiang University
Hangzhou, China
19 h-index
128 publications
4.9K citations

Cedars-Sinai Medical Center
Los Angeles, United States
18 h-index
63 publications
11.6K citations
Children's Hospital of Zhejiang University
Hangzhou, China
13 h-index
73 publications
2.5K citations

Chinese PLA General Hospital
Beijing, China
12 h-index
84 publications
3.9K citations
The University of Tokyo
Tokyo, Japan
11 h-index
44 publications
3.3K citations
1–8 of 609
BBRC · 23 publications · 852 citations
20
h-index
12 publications · 866 citations
12
h-index
JBC · 11 publications · 672 citations
11
h-index
11 publications · 528 citations
11
h-index
10 publications · 638 citations
10
h-index
1–5