Complex neurologic syndrome associated with the G1606A mutation of mitochondrial DNA

Archives of Neurology

Volumn 59, Issue 6, 2002, Pages 1013-1015

  Sacconi, Sabrina ^a,b   Salviati, Leonardo ^a,c   Gooch, Clifton ^a   Bonilla, Eduardo ^a   Shanske, Sara ^a   DiMauro, Salvatore ^a  

^a Och Spine at New York Presbyterian Hospitals   (United States)

^b UNIVERSITY OF MODENA AND REGGIO EMILIA   (Italy)

^c UNIVERSITY OF PADOVA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CITRATE SYNTHASE; CYTOCHROME C OXIDASE; MITOCHONDRIAL DNA; TRANSFER RNA;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; BASAL GANGLION; BLOOD SAMPLING; BRAIN ATROPHY; CASE REPORT; CLINICAL FEATURE; COMPLEX NEUROLOGIC SYNDROME; ENZYME ACTIVATION; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC SCREENING; GENOTYPE; HUMAN; MALE; NEUROLOGIC DISEASE; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE SEQUENCE; PATHOGENICITY; PHENOTYPE; PRIORITY JOURNAL; RESPIRATORY CHAIN; SKELETAL MUSCLE;

EID: 0036279552     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.59.6.1013     Document Type: Article

References (11)

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10. Ser(UCN) gene detected in a family with MERRF/MELAS overlap syndrome
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