Minisequencing mitochondrial DNA pathogenic mutations

BMC Medical Genetics

Volumn 9, Issue , 2008, Pages

  Álvarez Iglesias, Vanesa ^a   Barros, Francisco ^a   Carracedo, Ángel ^a   Salas, Antonio ^a  

^a UNIVERSITY OF SANTIAGO DE COMPOSTELA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA; PRIMER DNA;

ARTICLE; CLINICAL ARTICLE; DNA SEQUENCE; FISHER EXACT TEST; GENE AMPLIFICATION; GENE MUTATION; GENETIC ANALYSIS; GENETIC SCREENING; GENOME; GENOTYPE; HUMAN; MITOCHONDRIAL DNA DISORDER; MUTANT; POLYMERASE CHAIN REACTION; GENETICS; LEBER HEREDITARY OPTIC NEUROPATHY; LEIGH DISEASE; MELAS SYNDROME; METHODOLOGY; NUCLEOTIDE SEQUENCE; POINT MUTATION; SINGLE NUCLEOTIDE POLYMORPHISM; SPAIN;

DNA MUTATIONAL ANALYSIS; DNA PRIMERS; DNA, MITOCHONDRIAL; HUMANS; LEIGH DISEASE; MELAS SYNDROME; OPTIC ATROPHY, HEREDITARY, LEBER; POINT MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE; SPAIN;

EID: 43349091257     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-9-26     Document Type: Article

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