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The neurogenic weakness, ataxia and retinitis pigmentosa (NARP) syndrome mtDNA mutation (T8993G) triggers muscle ATPase deficiency and hypocitrullinaemia

✍ Scribed by B. Parfait; P. de Lonlay; J. C. von Kleist-Retzow; V. Cormier-Daire; D. Chrétien; A. Rötig; D. Rabier; J. M. Saudubray; P. Rustin; A. Munnich

Book ID: 106122835
Publisher: Springer
Year: 1999
Tongue: English
Weight: 100 KB
Volume: 158
Category: Article
ISSN: 0340-6997
DOI: 10.1007/s004310051009

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