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Volumn 16, Issue 5, 2015, Pages 541-544
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Risks inherent to mitochondrial replacement
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Author keywords
[No Author keywords available]
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Indexed keywords
CELL NUCLEUS DNA;
MITOCHONDRIAL DNA;
ALLELE;
DISORDERS OF MITOCHONDRIAL FUNCTIONS;
DONOR;
GENE;
GENE MUTATION;
GENETIC VARIABILITY;
GENOME;
GENOTYPE;
HAPLOTYPE;
HUMAN;
INVERTEBRATE MODEL;
LETTER;
MITOCHONDRIAL HAPLOGROUP;
MITOCHONDRIAL REPLACEMENT;
MITOCHONDRION;
MUTATION;
NATURAL SELECTION;
NONHUMAN;
OOCYTE;
PHENOTYPE;
PHYSICIAN;
PREDICTION;
PRIORITY JOURNAL;
PROGENY;
REPRODUCTION;
RISK;
SUBSTITUTION THERAPY;
X CHROMOSOME;
ANIMAL;
GENETIC VARIATION;
GENETICS;
METABOLISM;
MITOCHONDRIAL DISEASES;
ANIMALS;
DNA, MITOCHONDRIAL;
GENETIC VARIATION;
HUMANS;
MITOCHONDRIA;
MITOCHONDRIAL DISEASES;
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EID: 84928892969
PISSN: 1469221X
EISSN: 14693178
Source Type: Journal
DOI: 10.15252/embr.201439110 Document Type: Letter |
Times cited : (40)
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References (45)
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