A. Ruiz

Does the SLC40A1 gene modify HFE-related haemochromatosis phenotypes?

M. Baiget, A. Esteve, Á. Remacha, 2009, Annals of Hematology.

Mutations in HAMP and HJV genes and their impact on expression of clinical hemochromatosis in a cohort of 100 Spanish patients homozygous for the C282Y mutation of HFE gene

M. Baiget, A. Esteve, Á. Remacha, 2009, Annals of Hematology.

The relationship between iron overload and clinical characteristics in a Spanish cohort of 100 C282Y homozygous hemochromatosis patients

M. Baiget, A. Esteve, Á. Remacha, 2007, Annals of Hematology.

Prevalence of the C282Y, H63D, and S65C mutations of the HFE gene in 1,146 newborns from a region of Northern Spain.

M. Barceló, M. Baiget, C. Castell, 2004, Genetic testing.

Secondary coenzyme Q10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders.

P. Navas, E. Ruiz-Pesini, E. Trevisson, 2016, Mitochondrion.

Mutation analysis of GABRR1 andGABRR2 in autosomal recessive retinitis pigmentosa (RP25)

S. Borrego, G. Antiñolo, G. Cutting, 2000, Journal of medical genetics.

Análisis molecular del gen RPE65 en 72 familias españolas con retinitis pigmentaria autosómica recesiva

S. Borrego, G. Antiñolo, M. Baiget, 2001 .