z-logo
Premium
Detection of the A to G( 3243 ) mutation of mitochondrial DNA in Japanese families with mitochondrial encephalomyopathies
Author(s) -
Inui K.,
Tsukamoto H.,
Fukushima H.,
Taniike M.,
Tanaka J.,
Nishigaki T.,
Okada S.
Publication year - 1992
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1007/bf02435964
Subject(s) - medical school , medicine , pediatrics , mitochondrial encephalomyopathies , university hospital , family medicine , mitochondrial dna , medical education , genetics , biology , mitochondrial myopathy , gene

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom