Mitochondrial tRNACys gene mutation (A5814G): a second family with mitochondrial encephalopathy-Reference-Cited by-同舟云学术

Mitochondrial tRNACys gene mutation (A5814G): a second family with mitochondrial encephalopathy

Published:1997-05 Issue:3 Volume:7 Page:156-159
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Santorelli Filippo M.,Siciliano Gabriele,Casali Carlo,Basirico Matthew G.,Carrozzo Rosalba,Calvosa Fausta,Sartucci Ferdinando,Bonfiglio Luca,Murri Luigi,DiMauro Salvatore

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference16 articles.

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3. Mitochondrial DNA mutations associated with Leber's hereditary optic neuropathy;Wallace;Science,1988

4. Identification of a mutation in the mitochondrial tRNACys gene associated with mitochondrial encephalopathy;Manfredi;Hum Mut,1996

5. Evoked potentials in the evaluation of patients with mitochondrial myopathy;Sartucci;Eur Neurol,1993

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