A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness
Year: 1994
Type: article
Study design: Observational Study
Source: Human Mutation
Institutions: University of Glasgow, Glasgow Victoria Infirmary
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
Funder: Royal Society
OpenAlex ID: W2000610554