Results
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81.
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Homoplasmy, heteroplasmy, and mitochondrial dystonia. [electronic resource] by
- McFarland, R
- Chinnery, P F
- Blakely, E L
- Schaefer, A M
- Morris, A A M
- Foster, S M
- Tuppen, H A L
- Ramesh, V
- Dorman, P J
- Turnbull, D M
- Taylor, R W
Producer: 20070928
In:
Neurology vol. 69
Availability: No items available.
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82.
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Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiency. [electronic resource] by
- Olpin, S E
- Afifi, A
- Clark, S
- Manning, N J
- Bonham, J R
- Dalton, A
- Leonard, J V
- Land, J M
- Andresen, B S
- Morris, A A
- Muntoni, F
- Turnbull, D
- Pourfarzam, M
- Rahman, S
- Pollitt, R J
Producer: 20040617
In:
Journal of inherited metabolic disease vol. 26
Availability: No items available.
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83.
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Deficiency of respiratory chain complex I is a common cause of Leigh disease. [electronic resource] by
- Morris, A A
- Leonard, J V
- Brown, G K
- Bidouki, S K
- Bindoff, L A
- Woodward, C E
- Harding, A E
- Lake, B D
- Harding, B N
- Farrell, M A
- Bell, J E
- Mirakhur, M
- Turnbull, D M
Producer: 19960821
In:
Annals of neurology vol. 40
Availability: No items available.
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84.
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Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and children. [electronic resource] by
- Stewart, J D
- Tennant, S
- Powell, H
- Pyle, A
- Blakely, E L
- He, L
- Hudson, G
- Roberts, M
- du Plessis, D
- Gow, D
- Mewasingh, L D
- Hanna, M G
- Omer, S
- Morris, A A
- Roxburgh, R
- Livingston, J H
- McFarland, R
- Turnbull, D M
- Chinnery, P F
- Taylor, R W
Producer: 20090521
In:
Journal of medical genetics vol. 46
Availability: No items available.
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