M. Madrange
发表
J. Jais,
Y. Hamel,
François-Xavier Mauvais,
2018,
Molecular genetics and metabolism.
Biallelic loss-of-function OBSCN variants predispose individuals to severe, recurrent rhabdomyolysis
A. Forrest,
G. Ravenscroft,
N. Laing,
2021,
bioRxiv.
A. Smahi,
F. Tubach,
F. Derouin,
2020,
The Journal of allergy and clinical immunology.
A. Smahi,
J. Casanova,
A. Lim,
2019,
Experimental dermatology.
Y. Hamel,
M. Alfò,
P. de Lonlay,
2017,
Journal of Lipid Research.
G. Gyapay,
A. Smahi,
C. Bodemer,
2017,
Nature Medicine.
A. Smahi,
X. Pei,
Y. Hamel,
2016,
The Journal of investigative dermatology.
A. Smahi,
C. Bodemer,
A. Munnich,
2018,
The Journal of allergy and clinical immunology.
P. van Endert,
M. Polak,
N. Boddaert,
2020,
Journal of inherited metabolic disease.
P. van Endert,
Y. Hamel,
M. Rodero,
2021,
Cell reports. Medicine.
Thomas Meitinger,
Nathalie Boddaert,
Robert Barouki,
2017,
American journal of human genetics.
A. Smahi,
S. Duchatelet,
A. Hovnanian,
2019,
The British journal of dermatology.
A. Smahi,
P. Wolkenstein,
E. Sbidian,
2019,
The British journal of dermatology.
A. Smahi,
C. Bodemer,
A. Munnich,
2018,
The Journal of allergy and clinical immunology.