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Termination of damaged protein repair defines the occurrence of symptoms in carriers of the m.3243A > G tRNA(Leu) mutation. [electronic resource] by
- van Eijsden, R G E
- Eijssen, L M T
- Lindsey, P J
- van den Burg, C M M
- de Wit, L E A
- Rubio-Gozalbo, M E
- de Die, C E M
- Ayoubi, T
- Sluiter, W
- de Coo, I F M
- Smeets, H J M
Producer: 20080919
In:
Journal of medical genetics vol. 45
Availability: No items available.
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Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome. [electronic resource] by
- Gerards, M
- Sluiter, W
- van den Bosch, B J C
- de Wit, L E A
- Calis, C M H
- Frentzen, M
- Akbari, H
- Schoonderwoerd, K
- Scholte, H R
- Jongbloed, R J
- Hendrickx, A T M
- de Coo, I F M
- Smeets, H J M
Producer: 20101124
In:
Journal of medical genetics vol. 47
Availability: No items available.
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