CPEO and KSS differ in the percentage and location of the mtDNA deletion

Mitochondrion

Volumn 9, Issue 5, 2009, Pages 314-317

  López Gallardo, Ester ^a,b   López Pérez, Manuel J ^a,b   Montoya, Julio ^a,b,c   Ruiz Pesini, Eduardo ^a,b,c,d  

^a UNIVERSITY OF ZARAGOZA   (Spain)

^b CENTRO DE INVESTIGACIÓN BIOMÉDICA EN RED DE ENFERMEDADES RARAS CIBERER   (Spain)

^c INSTITUTO ARAGONÉS DE CIENCIAS DE LA SALUD   (Spain)

^d FUNDACIÓN ARAID   (Spain)

Author keywords

CPEO; Deletion; KSS; mtDNA; PS

Indexed keywords

MITOCHONDRIAL DNA;

ARTICLE; CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA; COHORT ANALYSIS; GENE DELETION; GENOTYPE; HUMAN; KEARNS SAYRE SYNDROME; MOLECULAR MECHANICS; MUSCLE BIOPSY; PHENOTYPE; PRIORITY JOURNAL; SOUTHERN BLOTTING;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; DNA, MITOCHONDRIAL; FEMALE; HUMANS; KEARNS-SAYER SYNDROME; MALE; OPHTHALMOPLEGIA, CHRONIC PROGRESSIVE EXTERNAL; SEQUENCE DELETION; YOUNG ADULT;

EID: 70149122589     PISSN: 15677249     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mito.2009.04.005     Document Type: Article

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