Familiar chronic progressive external ophthalmoplegia of mitochondrial origin;Oftalmoplejía crónica progresiva externa familiar de origen mitocondrial

Revista de Neurologia

Volumn 38, Issue 11, 2004, Pages 1023-1027

  Pineda, M ^a   Playan Ariso A ^c   Alcaine Villarroya, M J ^c   Vernet, A M ^a   Serra Castanera, A ^a   Solano, A ^c,e   Vilaseca, M A ^a   Artuch, R ^a   Lopez Perez M ^c   Briones Godino, M P ^b   Andrea, A ^d   Montoya, Julio ^c  

^a HOSPITAL SANT JOAN DE DÉU   (Spain)

^b Institut de Bioquimica Clinica Barcelona   (Spain)

^c UNIVERSITY OF ZARAGOZA   (Spain)

^d Ctro Invest Bioquim/Biol Molec   (Spain)

^e UNIVERSIDAD AUTÓNOMA DEL ESTADO DE MORELOS   (Mexico)

Author keywords

Deletion; Familiar chronic progressive external ophthalmoplegia; Mitochondrial DNA disorders

Indexed keywords

MITOCHONDRIAL DNA;

ARTICLE; CASE REPORT; CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA; DISORDERS OF MITOCHONDRIAL FUNCTIONS; EXTRACHROMOSOMAL INHERITANCE; EXTRAOCULAR MUSCLE; GENE DELETION; GENETIC ANALYSIS; HUMAN; MALE; PHENOTYPE; PRESCHOOL CHILD; PTOSIS; SKELETAL MUSCLE;

EID: 3843115466     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: 10.33588/rn.3811.2004019     Document Type: Article

References (17)

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