Fifteen novel mutations in the mitochondrial NADH dehydrogenase subunit 1, 2, 3, 4, 4L, 5 and 6 genes from Iranian patients with Leber's hereditary optic neuropathy (LHON)

Molecular Biology Reports

Volumn 40, Issue 12, 2013, Pages 6837-6841

  Rezvani, Zahra ^a   Didari, Elmira ^b   Arastehkani, Ahoura ^c   Ghodsinejad, Vadieh ^c   Aryani, Omid ^c   Kamalidehghan, Behnam ^d   Houshmand, Massoud ^b,c  

^a UNIVERSITY OF KASHAN   (Iran)

^b NATIONAL INSTITUTE OF GENETIC ENGINEERING AND BIOTECHNOLOGY   (Iran)

^c Special Medical Center Iran   (Iran)

^d UNIVERSITY OF MALAYA   (Malaysia)

Author keywords

Iranian patients with LHON; Leber's hereditary optic neuropathy; Mitochondrial DNA (mtDNA); ND genes

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CLINICAL ARTICLE; DNA POLYMORPHISM; DNA SEQUENCE; GENE MUTATION; HUMAN; IRAN; LEBER HEREDITARY OPTIC NEUROPATHY; MALE; MISSENSE MUTATION; MITOCHONDRIAL GENE; MITOCHONDRIAL GENOME; NADH DEHYDROGENASE SUBUNIT 1 GENE; NADH DEHYDROGENASE SUBUNIT 2 GENE; NADH DEHYDROGENASE SUBUNIT 3 GENE; NADH DEHYDROGENASE SUBUNIT 4 GENE; NADH DEHYDROGENASE SUBUNIT 4L GENE; NADH DEHYDROGENASE SUBUNIT 5 GENE; NADH DEHYDROGENASE SUBUNIT 6 GENE; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION;

GENETIC PREDISPOSITION TO DISEASE; HUMANS; IRAN; MALE; MITOCHONDRIA; MUTATION; NADH DEHYDROGENASE; OPTIC ATROPHY, HEREDITARY, LEBER; POLYMERASE CHAIN REACTION; PROTEIN SUBUNITS; YOUNG ADULT;

EID: 84890433212     PISSN: 03014851     EISSN: 15734978     Source Type: Journal    
DOI: 10.1007/s11033-013-2801-2     Document Type: Article

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