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Heterozygous deletion of TYMP and SCO2 genes in combination with c.261C > T mutation in TYMP as a cause of MNGIE

✍ Scribed by Markéta Tesařová⁎; Kamila Vinšová; Vendula Kučerová; Hana Hansíková; Tomáš Honzík; Jakub Krijt; Eva Karásková; Vratislav Smolka; Jiří Zeman

Book ID: 116752132
Publisher: Elsevier Science
Year: 2011
Tongue: English
Weight: 68 KB
Volume: 11
Category: Article
ISSN: 1567-7249
DOI: 10.1016/j.mito.2011.03.034

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Heterozygous deletion of TYMP and SCO2 genes in combination with c.261C&#xa0;>&#xa0;T mutation in TYMP as a cause of MNGIE

Heterozygous deletion of TYMP and SCO2 genes in combination with c.261C > T mutation in TYMP as a cause of MNGIE