A novel variation in the Twinkle linker region causing late-onset dementia

Neurogenetics

Volumn 11, Issue 1, 2010, Pages 21-25

  Echaniz Laguna, Andoni ^a   Chanson, Jean Baptiste ^a   Wilhelm, Jean Marie ^b   Sellal, François ^c   Mayençon, Martine ^d   Mohr, Michel ^e   Tranchant, Christine ^a   De Camaret, Bénédicte Mousson ^d  

^a HÔPITAL CIVIL   (France)

^b Centre Hospitalier Régional   (France)

^c Pasteur Hospital   (France)

^d HOSPICES CIVILS DE LYON   (France)

^e HÔPITAL DE HAUTEPIERRE   (France)

Author keywords

Chronic progressive external ophthalmoplegia; Dementia; Mitochondrial disease; Myopathy; PEO1; Twinkle

Indexed keywords

HELICASE; MITOCHONDRIAL DNA;

ADULT; AGED; ALZHEIMER DISEASE; ARTICLE; BRAIN FUNCTION; CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA; CLINICAL ARTICLE; CLINICAL FEATURE; DEMENTIA; DYSPHAGIA; DYSPHONIA; FEMALE; GENE; GENETIC VARIABILITY; GENOTYPE; HEARING LOSS; HUMAN; MALE; MYOPATHY; PATHOGENESIS; PEDIGREE; PEO1 GENE; PRIORITY JOURNAL; SENSORY NEUROPATHY;

ADULT; AGE OF ONSET; AGED; AGED, 80 AND OVER; DEMENTIA; DNA HELICASES; DNA, MITOCHONDRIAL; FEMALE; GENES, DOMINANT; HUMANS; MALE; MITOCHONDRIAL DISEASES; MUSCULAR DISEASES; NEUROPHYSIOLOGY; OPHTHALMOPLEGIA, CHRONIC PROGRESSIVE EXTERNAL; PEDIGREE;

EID: 76549093888     PISSN: 13646745     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10048-009-0202-4     Document Type: Article

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