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Mutation-free baby born from a mitochondrial encephalopathy, lactic acidosis and stroke-like syndrome carrier after blastocyst trophectoderm preimplantation genetic diagnosis

Björn Heindryckx (UGent) , Jitesh Neupane (UGent) , Mado Vandewoestyne (UGent) , CHRISTODOULOS CHRISTODOULOU (UGent) , Yens Jackers (UGent) , Jan Gerris (UGent) , Etienne Van den Abbeel (UGent) , Rudy Van Coster (UGent) , Dieter Deforce (UGent) and Petra De Sutter (UGent)
(2014) MITOCHONDRION. 18. p.12-17
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Keywords
Trophectoderm biopsy, TRNALEU(UUR) POINT MUTATION, Preimplantation genetic diagnosis (PGD), Heteroplasmy, Mitochondrial DNA (mtDNA), Blastocyst, POLAR BODIES, MTDNA, SEGREGATION, DISEASES, OOCYTES, EMBRYOS, PGD, THERAPY, PATIENT

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Chicago
Heindryckx, Björn, Jitesh Neupane, Mado Vandewoestyne, CHRISTODOULOS CHRISTODOULOU, Yens Jackers, Jan Gerris, Etienne Van den Abbeel, Rudy Van Coster, Dieter Deforce, and Petra De Sutter. 2014. “Mutation-free Baby Born from a Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-like Syndrome Carrier After Blastocyst Trophectoderm Preimplantation Genetic Diagnosis.” Mitochondrion 18: 12–17.
APA
Heindryckx, B., Neupane, J., Vandewoestyne, M., CHRISTODOULOU, C., Jackers, Y., Gerris, J., Van den Abbeel, E., et al. (2014). Mutation-free baby born from a mitochondrial encephalopathy, lactic acidosis and stroke-like syndrome carrier after blastocyst trophectoderm preimplantation genetic diagnosis. MITOCHONDRION, 18, 12–17.
Vancouver
1.
Heindryckx B, Neupane J, Vandewoestyne M, CHRISTODOULOU C, Jackers Y, Gerris J, et al. Mutation-free baby born from a mitochondrial encephalopathy, lactic acidosis and stroke-like syndrome carrier after blastocyst trophectoderm preimplantation genetic diagnosis. MITOCHONDRION. 2014;18:12–7.
MLA
Heindryckx, Björn, Jitesh Neupane, Mado Vandewoestyne, et al. “Mutation-free Baby Born from a Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-like Syndrome Carrier After Blastocyst Trophectoderm Preimplantation Genetic Diagnosis.” MITOCHONDRION 18 (2014): 12–17. Print.
@article{5828777,
  author       = {Heindryckx, Bj{\"o}rn and Neupane, Jitesh and Vandewoestyne, Mado and CHRISTODOULOU, CHRISTODOULOS and Jackers, Yens and Gerris, Jan and Van den Abbeel, Etienne and Van Coster, Rudy and Deforce, Dieter and De Sutter, Petra},
  issn         = {1567-7249},
  journal      = {MITOCHONDRION},
  keyword      = {Trophectoderm biopsy,TRNALEU(UUR) POINT MUTATION,Preimplantation genetic diagnosis (PGD),Heteroplasmy,Mitochondrial DNA (mtDNA),Blastocyst,POLAR BODIES,MTDNA,SEGREGATION,DISEASES,OOCYTES,EMBRYOS,PGD,THERAPY,PATIENT},
  language     = {eng},
  pages        = {12--17},
  title        = {Mutation-free baby born from a mitochondrial encephalopathy, lactic acidosis and stroke-like syndrome carrier after blastocyst trophectoderm preimplantation genetic diagnosis},
  url          = {http://dx.doi.org/10.1016/j.mito.2014.08.005},
  volume       = {18},
  year         = {2014},
}

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