Author Correction: Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations (Nature, (2016), 540, 7632, (270-275), 10.1038/nature20592);Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations

Nature

Volumn 540, Issue 7632, 2016, Pages 270-275

  Kang, Eunju ^a,b,j   Wu, Jun ^c   Gutierrez, Nuria Marti ^a,b   Koski, Amy ^a,b   Tippner Hedges, Rebecca ^a,b   Agaronyan, Karen ^d   Platero Luengo, Aida ^c   Martinez Redondo, Paloma ^c   Ma, Hong ^a,b   Lee, Yeonmi ^a,b   Hayama, Tomonari ^a,b   Van Dyken, Crystal ^a,b   Wang, Xinjian ^e   Luo, Shiyu ^e   Ahmed, Riffat ^a,b   Li, Ying ^a,b   Ji, Dongmei ^a,f   Kayali, Refik ^g   Cinnioglu, Cengiz ^g   Olson, Susan ^a   Jensen, Jeffrey ^a   Battaglia, David ^a   Lee, David ^a   Wu, Diana ^a   Huang, Taosheng ^e   Wolf, Don P ^a,b   Temiakov, Dmitry ^d   Belmonte, Juan Carlos Izpisua ^c   Amato, Paula ^a   Mitalipov, Shoukhrat ^a,b,h,i   more..

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^c SALK INSTITUTE FOR BIOLOGICAL STUDIES   (United States)

^d ROWAN UNIVERSITY   (United States)

^e CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

^f ANHUI MEDICAL UNIVERSITY   (China)

^g IVIGEN Los Angeles   (United States)

^h OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

ⁱ Oregon Health and Science University Department of Biomedical Engineering   (United States)

^j Asan Medical Center   (South Korea)

more..

Author keywords

[No Author keywords available]

Indexed keywords

CHORIONIC GONADOTROPIN; ESTRADIOL; MITOCHONDRIAL DNA; PROGESTERONE;

CELLS AND CELL COMPONENTS; DISEASE SEVERITY; GENE EXPRESSION; GROWTH; MITOCHONDRIAL DNA; MITOCHONDRION; MUTATION; PATHOGEN; POLYMORPHISM;

ADULT; ANTRAL FOLLICLE; ARTICLE; BLASTOCYST; CELL DIFFERENTIATION; CHILD; COMPARATIVE GENOMIC HYBRIDIZATION; CONSERVED SEQUENCE; CONTROLLED STUDY; COPY NUMBER VARIATION; EMBRYO; EMBRYO TRANSFER; EMBRYONIC STEM CELL; ESTRADIOL BLOOD LEVEL; FEMALE; GENE MUTATION; GERMLINE MUTATION; HAPLOTYPE; HUMAN; HUMAN CELL; HUMAN TISSUE; INTRACYTOPLASMIC SPERM INJECTION; LEIGH DISEASE; MALE; MEIOTIC SPINDLE; MELAS SYNDROME; METAPHASE; MITOCHONDRIAL DNA DISORDER; MITOCHONDRIAL DNA REPLICATION; MITOCHONDRIAL GENOME; MITOCHONDRIAL REPLACEMENT THERAPY; OOCYTE; OVARIAN RESERVE; OXIDATIVE PHOSPHORYLATION; PRESCHOOL CHILD; PRIORITY JOURNAL; PROGESTERONE BLOOD LEVEL; SCHOOL CHILD; YOUNG ADULT; BIOSYNTHESIS; CELL LINE; CYTOLOGY; EXTRACHROMOSOMAL INHERITANCE; GENETIC POLYMORPHISM; GENETICS; MEIOSIS; METABOLISM; MITOCHONDRIAL DISEASES; MUTATION; OOCYTE DONATION; PATHOLOGY; PEDIGREE; PROCEDURES;

UNITED STATES;

BLASTOCYST; CELL LINE; CONSERVED SEQUENCE; DNA, MITOCHONDRIAL; EMBRYONIC STEM CELLS; FEMALE; HAPLOTYPES; HUMANS; MALE; MATERNAL INHERITANCE; MEIOSIS; MITOCHONDRIAL DISEASES; MITOCHONDRIAL REPLACEMENT THERAPY; MUTATION; OOCYTE DONATION; OOCYTES; OXIDATIVE PHOSPHORYLATION; PEDIGREE; POLYMORPHISM, GENETIC;

EID: 85016726741     PISSN: 00280836     EISSN: 14764687     Source Type: Journal    
DOI: 10.1038/s41586-019-0876-1     Document Type: Erratum

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