Partha S. Ghosh
发表
A. O’Donnell-Luria,
L. Kunkel,
P. Kang,
2022,
Annals of clinical and translational neurology.
G. Comi,
C. Palermo,
M. Pane,
2022,
The Lancet Neurology.
Tonatiuh V Mendoza,
L. Kunkel,
François Modave,
2019,
Molecular genetics & genomic medicine.
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.
M. Milone,
Partha S. Ghosh,
2015,
Muscle & nerve.
P. Ghosh,
F. Al-Ghamdi,
Partha S. Ghosh,
2018,
Muscle & nerve.
J. Hoenicka,
A. Mammen,
Vijay Ganesh,
2022,
Neuromuscular Disorders.
A. Boon,
J. Mandrekar,
Partha S. Ghosh,
2017,
Muscle & nerve.
H. Lidov,
Partha S. Ghosh,
Luisa F Angel Buitrago,
2022,
Journal of clinical neuromuscular disease.
R. J. Ramamurthi,
S. Y. Kim,
H. Y. Wang,
2017,
The New England journal of medicine.
E. Estrella,
D. Ebrahimi-Fakhari,
Afshin Saffari,
2022,
American journal of medical genetics. Part A.
D. Goldstein,
A. Allen,
T. Strom,
2018,
The EMBO journal.
J. Hoenicka,
A. Mammen,
Vijay Ganesh,
2023,
Acta Neuropathologica.