2016

1. Generation of a human control iPSC line with a European mitochondrial haplogroup U background

   Stem Cell Research, Vol. 16, Núm. 1, pp. 88-91

2. Generation of a human iPSC line from a patient with Leigh syndrome

   Stem Cell Research, Vol. 16, Núm. 1, pp. 63-66

3. Generation of a human iPSC line from a patient with Leigh syndrome caused by a mutation in the MT-ATP6 gene

   Stem Cell Research, Vol. 16, Núm. 3, pp. 766-769

4. Generation of a human iPSC line from a patient with a defect of intergenomic communication

   Stem Cell Research, Vol. 16, Núm. 1, pp. 120-123

5. Generation of a human iPSC line from a patient with a mitochondrial encephalopathy due to mutations in the GFM1 gene

   Stem Cell Research, Vol. 16, Núm. 1, pp. 124-127

6. Generation of a human iPSC line from a patient with an optic atrophy 'plus' phenotype due to a mutation in the OPA1 gene

   Stem Cell Research, Vol. 16, Núm. 3, pp. 673-676