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1.
Phenotypic spectrum and clinical course of single large-scale mitochondrial DNA deletion disease in the paediatric population: a multicentre study.
J Med Genet
; 60(1): 65-73, 2023 01.
Article
in English
| MEDLINE | ID: mdl-34872991
2.
Broad phenotypic variability in patients with complex I deficiency due to mutations in NDUFS1 and NDUFV1.
Mitochondrion
; 21: 33-40, 2015 Mar.
Article
in English
| MEDLINE | ID: mdl-25615419
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