A New Mitochondrial Point Mutation in the Transfer RNALeu Gene in a Patient With a Clinical Phenotype Resembling Kearns-Sayre Syndrome
Seneca, Sara, Verhelst, Helene, De Meirleir, Linda, Meire, Françoise, Ceuterick-De Groote, Chantal, Lissens, Willy, Van Coster, RudyVolume:
58
Langue:
english
Journal:
Archives of Neurology
DOI:
10.1001/archneur.58.7.1113
Date:
July, 2001
Fichier:
PDF, 878 KB
english, 2001
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