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Abnormal activity of membrane phospholipid synthetic enzymes in the brain of patients with Friedreich's ataxia and spinocerebellar atrophy type-1. [electronic resource] by
- Ross, B M
- Eder, K
- Moszczynska, A
- Mamalias, N
- Lamarche, J
- Ang, L
- Pandolfo, M
- Rouleau, G
- Kirchgessner, M
- Kish, S J
Producer: 20000609
In:
Movement disorders : official journal of the Movement Disorder Society vol. 15
Availability: No items available.
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60.
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Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation. [electronic resource] by
- Buiakova, O I
- Xu, J
- Lutsenko, S
- Zeitlin, S
- Das, K
- Das, S
- Ross, B M
- Mekios, C
- Scheinberg, I H
- Gilliam, T C
Producer: 20000127
In:
Human molecular genetics vol. 8
Availability: No items available.
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