243rd ENMC international workshop: Developing guidelines for management of reproductive options for families with maternally inherited mtDNA disease, Amsterdam, the Netherlands, 22-24 March 2019

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)725-733
Number of pages9
JournalNeuromuscular Disorders
Volume29
Issue number9
DOIs
Publication statusPublished - Sep 2019

Keywords

  • PREIMPLANTATION GENETIC DIAGNOSIS
  • MITOCHONDRIAL-DNA DISORDERS
  • HUMAN OOCYTES
  • MUTATIONS
  • SEGREGATION
  • PGD
  • TRANSMISSION
  • BOTTLENECK
  • HETEROPLASMY
  • REPLACEMENT

Cite this

@article{6d4fa9ab84424ae6a9bfe7456c652bcb,
title = "243rd ENMC international workshop: Developing guidelines for management of reproductive options for families with maternally inherited mtDNA disease, Amsterdam, the Netherlands, 22-24 March 2019",
keywords = "PREIMPLANTATION GENETIC DIAGNOSIS, MITOCHONDRIAL-DNA DISORDERS, HUMAN OOCYTES, MUTATIONS, SEGREGATION, PGD, TRANSMISSION, BOTTLENECK, HETEROPLASMY, REPLACEMENT",
author = "Joanna Poulton and Julie Steffann and Joerg Burgstaller and Robert McFarland and B. Arbeithuber and J. Bengoa and J. Burgstaller and S. Chan and M. Chiaratti and M. Crouch and R. Dimond and Enriques, {J. A.} and G. Gorman and L. Hyslop and I. Johnston and J. Kitto and A. Maguire and Robert McFarland and S. Mitalipov and Van Otterloo and J. Poulton and S. Sallevelt and H. Smeets and C. Spits and {St John}, J. and J. Steffann and J. Stewart and M. Stoneking and D. Thorburn and {van der Veer}, E. and D. Wells",
year = "2019",
month = "9",
doi = "10.1016/j.nmd.2019.08.004",
language = "English",
volume = "29",
pages = "725--733",
journal = "Neuromuscular Disorders",
issn = "0960-8966",
publisher = "Elsevier Science",
number = "9",

}

TY - JOUR

T1 - 243rd ENMC international workshop

T2 - Developing guidelines for management of reproductive options for families with maternally inherited mtDNA disease, Amsterdam, the Netherlands, 22-24 March 2019

AU - Poulton, Joanna

AU - Steffann, Julie

AU - Burgstaller, Joerg

AU - McFarland, Robert

AU - Arbeithuber, B.

AU - Bengoa, J.

AU - Burgstaller, J.

AU - Chan, S.

AU - Chiaratti, M.

AU - Crouch, M.

AU - Dimond, R.

AU - Enriques, J. A.

AU - Gorman, G.

AU - Hyslop, L.

AU - Johnston, I.

AU - Kitto, J.

AU - Maguire, A.

AU - McFarland, Robert

AU - Mitalipov, S.

AU - Otterloo, Van

AU - Poulton, J.

AU - Sallevelt, S.

AU - Smeets, H.

AU - Spits, C.

AU - St John, J.

AU - Steffann, J.

AU - Stewart, J.

AU - Stoneking, M.

AU - Thorburn, D.

AU - van der Veer, E.

AU - Wells, D.

PY - 2019/9

Y1 - 2019/9

KW - PREIMPLANTATION GENETIC DIAGNOSIS

KW - MITOCHONDRIAL-DNA DISORDERS

KW - HUMAN OOCYTES

KW - MUTATIONS

KW - SEGREGATION

KW - PGD

KW - TRANSMISSION

KW - BOTTLENECK

KW - HETEROPLASMY

KW - REPLACEMENT

U2 - 10.1016/j.nmd.2019.08.004

DO - 10.1016/j.nmd.2019.08.004

M3 - Article

VL - 29

SP - 725

EP - 733

JO - Neuromuscular Disorders

JF - Neuromuscular Disorders

SN - 0960-8966

IS - 9

ER -