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Cytochrome c oxidase deficiency in Leigh syndrome. [electronic resource] by
- DiMauro, S
- Servidei, S
- Zeviani, M
- DiRocco, M
- DeVivo, D C
- DiDonato, S
- Uziel, G
- Berry, K
- Hoganson, G
- Johnsen, S D
Producer: 19880304
In:
Annals of neurology vol. 22
Availability: No items available.
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Clinical and molecular features of mitochondrial DNA depletion syndromes. [electronic resource] by
- Spinazzola, A
- Invernizzi, F
- Carrara, F
- Lamantea, E
- Donati, A
- Dirocco, M
- Giordano, I
- Meznaric-Petrusa, M
- Baruffini, E
- Ferrero, I
- Zeviani, M
Producer: 20090716
In:
Journal of inherited metabolic disease vol. 32
Availability: No items available.
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A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy. [electronic resource] by
- Bruno, C
- DiRocco, M
- Lamba, L D
- Bado, M
- Marino, C
- Tsujino, S
- Shanske, S
- Stella, G
- Minetti, C
- van Diggelen, O P
- DiMauro, S
Producer: 19991123
In:
Neuromuscular disorders : NMD vol. 9
Availability: No items available.
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Prenatal diagnosis of Sjögren-Larsson syndrome using enzymatic methods. [electronic resource] by
- Rizzo, W B
- Craft, D A
- Kelson, T L
- Bonnefont, J P
- Saudubray, J M
- Schulman, J D
- Black, S H
- Tabsh, K
- Dirocco, M
- Gardner, R J
Producer: 19941216
In:
Prenatal diagnosis vol. 14
Availability: No items available.
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