K. Coffman
发表
R. Nardone,
L. Bansal,
G. Zuccoli,
2016,
Journal of child neurology.
J. Quezada,
K. Coffman,
Keith A. Coffman,
2018,
CNS Drugs.
Laurie D. Smith,
Neil A. Miller,
S. Kingsmore,
2015
.
M. Okun,
I. Malaty,
K. Müller-Vahl,
2022,
Journal of clinical medicine.
Deepti Nagesh,
K. Coffman,
Marcie Goeden,
2018,
Seminars in pediatric neurology.
P. Strick,
E. Hoshi,
B. Abler,
2015
.
Peter L Strick,
P. Strick,
R. Dum,
2011,
Proceedings of the National Academy of Sciences.
U. Surti,
A. Rajkovic,
J. Locker,
2021,
Molecular genetics & genomic medicine.
R. Forsyth,
T. Allison,
K. Coffman,
2017,
Journal of child neurology.
Laurie D. Smith,
Neil A. Miller,
S. Kingsmore,
2015,
Human mutation.
J. Jankovic,
K. Black,
J. Grant,
2018,
Movement disorders : official journal of the Movement Disorder Society.
Orion J. Buske,
Nigel J. Price,
Warren A. Cheung,
2021,
medRxiv.
R. Hickey,
Susan K. Yaeger,
K. Coffman,
2017,
Annals of emergency medicine.
A. Berg,
D. Gaebler-Spira,
K. Coffman,
2021,
Developmental medicine and child neurology.
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement
Beryl B. Cummings,
Carol J. Saunders,
C. Saunders,
2019,
Acta Neuropathologica.
D. Kondziolka,
E. Tyler-Kabara,
D. Crammond,
2011,
Journal of neurosurgery. Pediatrics.
R. Borgatti,
K. Coffman,
2020,
Neurology.
D. Gilbert,
Daniel A. N. Barbosa,
M. Kruer,
2022,
Journal of child neurology.
P. Strick,
R. Dum,
K. Coffman,
2012,
Proceedings of the National Academy of Sciences.
D. Doherty,
K. Coffman,
2020,
Neurology.