Work

In vitro and ex vivo suppression by aminoglycosides of PCDH15 nonsense mutations underlying type 1 Usher syndrome

Year: 2007

Type: article

Source: Human Genetics

DOI: 10.1007/s00439-007-0410-7

Authors: Annie Rebibo-Sabbah, Igor Nudelman, Zubair M. Ahmed, Timor Baasov, Tamar Ben-Yosef

Institutions: Technion – Israel Institute of Technology, Rappaport Family Institute for Research in the Medical Sciences, National Institutes of Health, National Institute on Deafness and Other Communication Disorders

Language: English

Topic: Retinal Development and Disorders

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: Mizutani Foundation for Glycoscience, National Institute on Deafness and Other Communication Disorders

Awards: Mapping And Cloning Hereditary Hearing Impairment Genes, Identification of Genes Causing Syndromic And Nonsyndromic Hearing Impairment

OpenAlex ID: W2042411797

FWCI: 2.254

Cites: 37

Cited by: 74

Related to: 10