Page last updated: 2024-08-17

nad and Hearing Loss, Sensorineural

nad has been researched along with Hearing Loss, Sensorineural in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	1 (100.00)	2.80

Authors

Authors	Studies
Ayuso, C; Banfi, S; Bedoni, N; Brunetti-Pierri, N; Cappuccio, G; Corton, M; Di Rocco, M; Filocamo, M; Lanza, F; Lualdi, S; Morana, G; Nigro, V; Pinelli, M; Quinodoz, M; Rivolta, C; Simonelli, F; Superti-Furga, A; Testa, F; Torella, A	1

Other Studies

1 other study(ies) available for nad and Hearing Loss, Sensorineural

Article	Year
An Alu-mediated duplication in NMNAT1, involved in NAD biosynthesis, causes a novel syndrome, SHILCA, affecting multiple tissues and organs. Human molecular genetics, 2020, 08-03, Volume: 29, Issue:13 Topics: Adolescent; Animals; Child; Child, Preschool; Disease Models, Animal; Exons; Genetic Predisposition to Disease; Hearing Loss, Sensorineural; Humans; Infant; Intellectual Disability; Leber Congenital Amaurosis; Male; Mice; Mutation; NAD; Nicotinamide-Nucleotide Adenylyltransferase; Osteochondrodysplasias; Pedigree; Retinal Degeneration	2020

Article

Year

An Alu-mediated duplication in NMNAT1, involved in NAD biosynthesis, causes a novel syndrome, SHILCA, affecting multiple tissues and organs.

Human molecular genetics, 2020, 08-03, Volume: 29, Issue:13

Topics: Adolescent; Animals; Child; Child, Preschool; Disease Models, Animal; Exons; Genetic Predisposition to Disease; Hearing Loss, Sensorineural; Humans; Infant; Intellectual Disability; Leber Congenital Amaurosis; Male; Mice; Mutation; NAD; Nicotinamide-Nucleotide Adenylyltransferase; Osteochondrodysplasias; Pedigree; Retinal Degeneration

2020