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Autosomal Recessive 77 Deafness

Also Known As:

Deafness, Autosomal Recessive 77; DFNB77

Networked: 3 relevant articles (0 outcomes, 1 trials/studies)

Disease Context: Research Results

Related Diseases

1.	Deafness (Deaf Mutism)
2.	Nonsyndromic Deafness
3.	Hearing Loss (Hearing Impairment)
4.	Autosomal Recessive 77 Deafness

Experts

1.	Dai, Pu: 1 article (01/2022)
2.	Gao, Xue: 1 article (01/2022)
3.	Han, Ming-Yu: 1 article (01/2022)
4.	Huang, Sha-Sha: 1 article (01/2022)
5.	Kang, Dong-Yang: 1 article (01/2022)
6.	Wang, Wei-Qian: 1 article (01/2022)
7.	Xu, Jin-Cao: 1 article (01/2022)
8.	Yang, Kun: 1 article (01/2022)
9.	Yang, Su-Yan: 1 article (01/2022)
10.	Yuan, Yong-Yi: 1 article (01/2022)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Autosomal Recessive 77 Deafness:

1.	DNA (Deoxyribonucleic Acid)IBA 09/01/2009 - "Based on the studies in mice, we screened DNA from human families segregating deafness and identified a mutation in LOXHD1, which causes DFNB77, a progressive form of autosomal-recessive nonsyndromic hearing loss (ARNSHL). "
2.	Lipoxygenase (Lipoxygenase-1)IBA 01/01/2022 - "The LOXHD1 gene (DFNB77), encoding lipoxygenase homology domain 1, is a rare hearing loss gene found in several populations. " 01/01/2019 - "Deafness, autosomal recessive 77 (DFNB77) is a rare non-syndromic hearing loss (NSHL) worldwide, which is caused by deleterious variants within lipoxygenase homology domains 1 (LOXHD1). "