Sven Günther
发表
J. Lippincott-Schwartz,
J. Winkler,
B. Winner,
2017,
The Journal of cell biology.
F. Limosin,
D. Lebeaux,
J. Hulot,
2021,
Frontiers in Psychiatry.
C. Beetz,
C. Hübner,
S. Biskup,
2018,
Human mutation.
N. Reinmuth,
L. Zender,
T. Ganzenmueller,
2022,
Frontiers in Oncology.
M. Simpson,
M. Patton,
R. Trembath,
2016,
Human mutation.
Identification of causative variants in TXNL4A in Burn-McKeown syndrome and isolated choanal atresia
R. Pfundt,
J. Hurst,
A. V. D. van den Ouweland,
2017,
European Journal of Human Genetics.
Ø. Braaten,
C. Beetz,
F. Wijburg,
2019,
Molecular genetics & genomic medicine.
F. Caixeta,
K. Kullander,
Manuela Schmidt,
2017,
bioRxiv.
F. Caixeta,
K. Kullander,
Manuela Schmidt,
2018,
Life Science Alliance.
P. Bauer,
R. Heller,
P. Ray,
2016
.
P. Bauer,
R. Heller,
P. Ray,
2016,
Human mutation.