Generation of an iPSC line of a patient with Angelman syndrome due to an imprinting defect.

Neureiter A, Brändl B, Hiber M, Tandon R, Müller FJ, Steenpass L

DOI: 10.1016/j.scr.2018.09.015
Published: 2018 Dec
Container: Stem cell research
Publisher: Not recorded
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1016/j.scr.2018.09.015,
  title = {Generation of an iPSC line of a patient with Angelman syndrome due to an imprinting defect.},
  author = {Neureiter A and Brändl B and Hiber M and Tandon R and Müller FJ and Steenpass L},
  year = {2018},
  journal = {Stem cell research},
  doi = {10.1016/j.scr.2018.09.015},
  url = {https://doi.org/10.1016/j.scr.2018.09.015}
}

RIS

TY  - JOUR
TI  - Generation of an iPSC line of a patient with Angelman syndrome due to an imprinting defect.
AU  - Neureiter A
AU  - Brändl B
AU  - Hiber M
AU  - Tandon R
AU  - Müller FJ
AU  - Steenpass L
PY  - 2018
JO  - Stem cell research
DO  - 10.1016/j.scr.2018.09.015
UR  - https://doi.org/10.1016/j.scr.2018.09.015
ER  -

APA

A, N., B, B., M, H., R, T., FJ, M., & L, S. (2018). Generation of an iPSC line of a patient with Angelman syndrome due to an imprinting defect.. Stem cell research. https://doi.org/10.1016/j.scr.2018.09.015

Source records

pubmed · retrieved 2026-09-25T05:23:54.315Z