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Genetic biochemical and pathophysiological characterization of a familial mitochondrial encephalomyopathy (MERRF). [electronic resource] by
- Seibel, P
- Degoul, F
- Bonne, G
- Romero, N
- François, D
- Paturneau-Jouas, M
- Ziegler, F
- Eymard, B
- Fardeau, M
- Marsac, C
Producer: 19920204
In:
Journal of the neurological sciences vol. 105
Availability: No items available.
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376.
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A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome. [electronic resource] by
- Barrientos, A
- Volpini, V
- Casademont, J
- Genís, D
- Manzanares, J M
- Ferrer, I
- Corral, J
- Cardellach, F
- Urbano-Márquez, A
- Estivill, X
- Nunes, V
Producer: 19960507
In:
The Journal of clinical investigation vol. 97
Availability: No items available.
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379.
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