- Tytuł:
- Concurrent AFG3L2 and SPG7 mutations associated with syndromic parkinsonism and optic atrophy with aberrant OPA1 processing and mitochondrial network fragmentation.
- Autorzy:
- Źródło:
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Human Mutation ; Dec2018, Vol. 39 Issue 12, p2060-2071, 12p
Czasopismo naukowe