P. Yun
发表
C. Bönnemann,
D. Cuadras,
C. Ortez,
2021,
Neurology.
Ronald M. Summers,
Jianhua Yao,
Andrew E. Arai,
2018,
2018 IEEE 15th International Symposium on Biomedical Imaging (ISBI 2018).
A. Arai,
C. Bönnemann,
S. Donkervoort,
2020,
Neuromuscular Disorders.
C. Bönnemann,
S. Donkervoort,
A. Foley,
2020,
BMC Pediatrics.
Jamie L. Marshall,
D. MacArthur,
M. Lek,
2019,
Journal of neuromuscular diseases.
E. Mercuri,
F. Muntoni,
T. Pierson,
2021,
Brain communications.
C. Bönnemann,
W. Zein,
A. Hoke,
2017,
Neurology: Genetics.
A. Arai,
C. Bönnemann,
A. Innes,
2019,
Neurology.
BET1 variants establish impaired vesicular transport as a cause for muscular dystrophy with epilepsy
Beryl B. Cummings,
C. Bönnemann,
M. Schwake,
2021,
EMBO molecular medicine.
W. Triplett,
C. Bönnemann,
D. Lott,
2020,
Journal of neuromuscular diseases.
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement
Beryl B. Cummings,
Carol J. Saunders,
C. Saunders,
2019,
Acta Neuropathologica.
T. Roberts,
C. Bönnemann,
D. Rifkin,
2023,
bioRxiv.
A. Arai,
L. Medne,
C. Bönnemann,
2023,
Annals of clinical and translational neurology.