The neurogenic weakness, ataxia and retinitis pigmentosa (NARP) syndrome mtDNA mutation (T8993G) triggers muscle ATPase deficiency and hypocitrullinaemia-Reference-Cited by-同舟云学术

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

Published:1999-01-01 Issue:1 Volume:158 Page:55-58
ISSN:0340-6199
Container-title:European Journal of Pediatrics
language:
Short-container-title:European Journal of Pediatrics

Author:

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

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s004310051009.pdf

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