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A family with Leigh syndrome caused by the rarer T8993C mutation
Author(s) -
Chakrapani A.,
Heptinstall L.,
Walter J.
Publication year - 1998
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 - 10.1023/a:1005401121344
Subject(s) - missense mutation , citation , mutation , genetics , point mutation , mitochondrial dna , genealogy , medicine , gene , library science , biology , computer science , history