A mitochondrial tRNAVal gene mutation (G1642A) in a patient...

Neurology 1998 / 01 Vol. 50; Iss. 1

A mitochondrial tRNAVal gene mutation (G1642A) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes

de Coo, I. F. M., Sistermans, E. A., de Wijs, I. J., Catsman-Berrevoets, C., Busch, H. F. M., Scholte, H. R., de Klerk, J. B. C., van Oost, B. A., Smeets, H. J. M.
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Volume:
50
Language:
english
Journal:
Neurology
DOI:
10.1212/WNL.50.1.293
Date:
January, 1998
File:
PDF, 501 KB
english, 1998
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