VIICTR
Profiles
ORIT
Pediatrics CRA
Home
About
Overview
Sharing Data
ORCID
Help
History (0)
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
Search Result Details
Back to Search Results
This page shows the details of why an item matched the keywords from your search.
Search Results
SCAGLIA, FERNANDO
One or more keywords matched the following items that are connected to
SCAGLIA, FERNANDO
Item Type
Name
Concept
Iron-Sulfur Proteins
Academic Article
Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy.
Academic Article
Mitochondrial energetic impairment in a patient with late-onset glutaric acidemia Type 2.
Search Criteria
Iron Sulfur Proteins