F. Leal
发表
E. Richard,
C. Pérez-Cerdá,
A. Ribes,
2009,
Human mutation.
M. Ugarte,
S. Ramón-Maiques,
A. Gámez,
2022,
Human mutation.
I. T. de Almeida,
X. de la Cruz,
C. Riera,
2018,
Orphanet Journal of Rare Diseases.
M. Ugarte,
L. Chabraoui,
B. Pérez,
2010,
Clinical biochemistry.
E. Richard,
C. Pérez-Cerdá,
B. Merinero,
2017
.
C. Pérez-Cerdá,
B. Merinero,
M. Ugarte,
2019,
European Journal of Human Genetics.
M. Ugarte,
M. L. Couce,
R. Yahyaoui,
2022,
International journal of molecular sciences.
T. K. Doktor,
Ulrika S S Petersen,
L. L. Holm,
2022,
Nucleic acid therapeutics.
E. Bermejo,
M. Ugarte,
E. Mansilla,
2006,
American journal of medical genetics. Part A.
C. Pérez-Cerdá,
B. Merinero,
M. Ugarte,
2018,
JIMD reports.
M. Ugarte,
B. Pérez,
C. Pedrón‐Giner,
2022,
Journal of clinical medicine.
Isolated and Combined Remethylation Disorders: Biochemical and Genetic Diagnosis and Pathophysiology
E. Richard,
C. Pérez-Cerdá,
B. Merinero,
2017
.
R. Banerjee,
E. Richard,
B. Merinero,
2015,
Clinical genetics.
Aurora Martínez,
M. Ugarte,
R. Artuch,
2020,
Human mutation.
C. Pérez-Cerdá,
B. Merinero,
M. Ugarte,
2019,
European Journal of Human Genetics.
M. Ugarte,
R. Artuch,
B. Pérez,
2022,
Clinical genetics.