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Occipital Horn Syndrome as a Result of Splice Site Mutations in ATP7A. No Activity of ATP7A Splice Variants Missing Exon 10 or Exon 15. / Møller, Lisbeth Birk; Mogensen, Mie; Weaver, David D.; Pedersen, Per Amstrup.
In:
Frontiers in Molecular Neuroscience, Vol. 14, 532291, 2021.
Research output: Contribution to journal › Journal article › Research › peer-review
Harvard
Møller, LB, Mogensen, M, Weaver, DD
& Pedersen, PA 2021, '
Occipital Horn Syndrome as a Result of Splice Site Mutations in ATP7A. No Activity of ATP7A Splice Variants Missing Exon 10 or Exon 15',
Frontiers in Molecular Neuroscience, vol. 14, 532291.
https://doi.org/10.3389/fnmol.2021.532291APA
Møller, L. B., Mogensen, M., Weaver, D. D.
, & Pedersen, P. A. (2021).
Occipital Horn Syndrome as a Result of Splice Site Mutations in ATP7A. No Activity of ATP7A Splice Variants Missing Exon 10 or Exon 15.
Frontiers in Molecular Neuroscience,
14, [532291].
https://doi.org/10.3389/fnmol.2021.532291Vancouver
Møller LB, Mogensen M, Weaver DD
, Pedersen PA.
Occipital Horn Syndrome as a Result of Splice Site Mutations in ATP7A. No Activity of ATP7A Splice Variants Missing Exon 10 or Exon 15.
Frontiers in Molecular Neuroscience. 2021;14. 532291.
https://doi.org/10.3389/fnmol.2021.532291Author
Møller, Lisbeth Birk ; Mogensen, Mie ; Weaver, David D. ; Pedersen, Per Amstrup. / Occipital Horn Syndrome as a Result of Splice Site Mutations in ATP7A. No Activity of ATP7A Splice Variants Missing Exon 10 or Exon 15. In: Frontiers in Molecular Neuroscience. 2021 ; Vol. 14.
Bibtex
@article{5510a5df1cd34dae9760c6d752335ab5,
title = "Occipital Horn Syndrome as a Result of Splice Site Mutations in ATP7A. No Activity of ATP7A Splice Variants Missing Exon 10 or Exon 15",
author = "M{\o}ller, {Lisbeth Birk} and Mie Mogensen and Weaver, {David D.} and Pedersen, {Per Amstrup}",
year = "2021",
doi = "10.3389/fnmol.2021.532291",
language = "English",
volume = "14",
journal = "Frontiers in Molecular Neuroscience",
issn = "1662-5099",
publisher = "Frontiers Research Foundation",
}
RIS
TY - JOUR
T1 - Occipital Horn Syndrome as a Result of Splice Site Mutations in ATP7A. No Activity of ATP7A Splice Variants Missing Exon 10 or Exon 15
AU - Møller, Lisbeth Birk
AU - Mogensen, Mie
AU - Weaver, David D.
AU - Pedersen, Per Amstrup
PY - 2021
Y1 - 2021
U2 - 10.3389/fnmol.2021.532291
DO - 10.3389/fnmol.2021.532291
M3 - Journal article
C2 - 33967692
VL - 14
JO - Frontiers in Molecular Neuroscience
JF - Frontiers in Molecular Neuroscience
SN - 1662-5099
M1 - 532291
ER -
