Frequency and clinical features of patients with sensorineural hearing loss associated with the A3243G mutation of the mitochondrial DNA in otorhinolaryngic clinics

1 October 2001

journal article
Published by Springer Nature in Journal of Human Genetics

Vol. 46 (10) , 595-599
https://doi.org/10.1007/s100380170027

Abstract

Journal of Human Genetics, official journal of the Japan Society of Human Genetics, publishes original articles and reviews on all aspects of human genetics, including medical genetics and genomics

Keywords

HUMAN GENETICS
CYTOGENETICS
MOLECULAR GENETICS
BIOCHEMICAL GENETICS
GENOMICS
POPULATION GENETICS
DEVELOPMENTAL GENETICS
CLINICAL GENETICS
HUMAN GENOME
PHARMACOGENETICS
STATISTICAL GENETICS
EPIGENETICS
GENETIC EPIDEMIOLOGY

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