Detalhe da pesquisa
1.
De novo pathogenic DNM1L variant in a patient diagnosed with atypical hereditary sensory and autonomic neuropathy.
Mol Genet Genomic Med
; 7(10): e00961, 2019 10.
Artigo
Inglês
| MEDLINE | ID: mdl-31475481
2.
Deoxyribonucleoside kinases in mitochondrial DNA depletion.
Nucleosides Nucleotides Nucleic Acids
; 23(8-9): 1205-15, 2004 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-15571232