Limitations of preimplantation genetic diagnosis for mitochondrial DNA diseases

Cell Reports

Volumn 7, Issue 4, 2014, Pages 935-937

  Mitalipov, Shoukhrat ^a,b   Amato, Paula ^b   Parry, Samuel ^c   Falk, Marni J ^c  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^c UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

DISEASE TRANSMISSION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC SCREENING; HETEROPLASMY; HUMAN; LACTIC ACIDEMIA; LETTER; MELAS SYNDROME; MITOCHONDRIAL DNA DISORDER; MITOCHONDRIAL GENOME; MUTATIONAL ANALYSIS; PHYSICAL EXAMINATION; POLYMERASE CHAIN REACTION; PREIMPLANTATION GENETIC DIAGNOSIS; PRIORITY JOURNAL; AMINO ACID SUBSTITUTION; ANGER; BEHAVIOR DISORDER; CENTRAL NERVOUS SYSTEM DISEASE; CLOSTRIDIUM DIFFICILE INFECTION; CYANOSIS; DEHYDRATION; DEVELOPMENTAL DISORDER; DNA DETERMINATION; FACE DYSMORPHIA; FEBRILE CONVULSION; FERTILIZATION IN VITRO; GASTROESOPHAGEAL REFLUX; HETERODUPLEX ANALYSIS; HETEROZYGOSITY; HYPERACTIVITY; HYPOGLYCEMIA; HYPOXEMIA; INFECTION SENSITIVITY; LACTIC ACIDOSIS; MITOCHONDRIAL GENETICS; MOTHER CHILD RELATION; MYELIN DEFICIENCY; NONHUMAN; PHOTOREACTIVITY; PLACENTA ATRESIA; PLACENTA DISORDER; PREECLAMPSIA; PRENATAL DIAGNOSIS; RESTRICTION MAPPING; VOMITING; ANIMAL; BLASTOCYST; CELL DIVISION; CYTOLOGY; EMBRYO DEVELOPMENT; EMBRYOLOGY; FEMALE; GENETICS; HAPLOTYPE; OOCYTE; PREGNANCY; RHESUS MONKEY;

ANIMALS; BLASTOCYST; CELL DIVISION; DNA, MITOCHONDRIAL; EMBRYONIC DEVELOPMENT; FEMALE; HAPLOTYPES; MACACA MULATTA; OOCYTES; PREGNANCY;

EID: 84901199108     PISSN: None     EISSN: 22111247     Source Type: Journal    
DOI: 10.1016/j.celrep.2014.05.004     Document Type: Letter

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