Associated Papers
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 19.19
Sequence variations in mitochondrial ferritin: distribution in healthy controls and different types of patients.
Castiglioni E et al.
Genetic Testing and Molecular Biomarkers, 2010
Select a paper to view details