K. Maincent
发表
E. Bourel-ponchel,
D. Ville,
A. Saâd,
2016,
Clinical genetics.
T. Billette de Villemeur,
B. Héron,
K. Maincent,
2018,
Orphanet Journal of Rare Diseases.
L. Servais,
J. Hogrel,
S. Quijano-roy,
2015,
PloS one.
L. Zitvogel,
J. Bénard,
D. Valteau‐Couanet,
2002,
Blood.
J. Dupont,
F. Letourneur,
K. Maincent,
2009,
American journal of medical genetics. Part A.
A. Afenjar,
D. Rodriguez,
T. Billette de Villemeur,
2020,
Neurology: Genetics.
A. Toutain,
N. Romero,
L. Pasquier,
2013,
European Journal of Human Genetics.
A. Toutain,
L. Pasquier,
S. Mercier,
2013,
European Journal of Human Genetics.
A. Toutain,
N. Romero,
L. Pasquier,
2013
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F. Rivier,
A. Toutain,
B. Echenne,
2010,
Annals of neurology.
S. Julia,
R. Touraine,
A. Afenjar,
2018,
Journal of Medical Genetics.
B. Gilbert-Dussardier,
M. Gonzalès,
B. Grandchamp,
2011,
Neuromuscular Disorders.
M. Zilbovicius,
C. Adamsbaum,
N. Boddaert,
2004,
American journal of medical genetics. Part A.
F. Lofaso,
B. Fauroux,
K. Maincent,
2011,
European Respiratory Journal.
K. Baumstarck,
P. Auquier,
L. Dany,
2022,
Scientific Reports.
K. Baumstarck,
A. Loundou,
P. Auquier,
2019,
Disability and health journal.
L. Servais,
J. Hogrel,
S. Quijano-roy,
2015,
PloS one.
T. Voit,
L. Servais,
S. Quijano-roy,
2013,
Neuromuscular Disorders.