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Gender-related penetrance and de novo GTP-cyclohydrolase I gene mutations in dopa-responsive dystonia. [electronic resource] by
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- Bird, T D
- Hunter, A
- Sadeh, M
- Tagawa, T
- St George-Hyslop, P H
- Guttman, M
- Morris, L W
- Hornykiewicz, O
- Shimadzu, M
- Kish, S J
Producer: 19980507
In:
Neurology vol. 50
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Expanded motor and psychiatric phenotype in autosomal dominant Segawa syndrome due to GTP cyclohydrolase deficiency. [electronic resource] by
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- Theys, P
- Wevers, R
- Romstad, A
- Møller, L B
- Hedrich, K
- Goriounov, D
- Blau, N
- Klein, C
- Casaer, P
Producer: 20060223
In:
Journal of neurology, neurosurgery, and psychiatry vol. 77
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769.
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Increased superoxide and endothelial NO synthase uncoupling in blood vessels of Bmal1-knockout mice. [electronic resource] by
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- Cheng, Bo
- Sharma, Shruti
- Kumar, Sanjiv
- Caldwell, R William
- Yao, Lin
- Ali, M Irfan
- Merloiu, Ana M
- Stepp, David W
- Black, Stephen M
- Fulton, David J R
- Rudic, R Daniel
Producer: 20130131
In:
Circulation research vol. 111
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775.
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776.
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777.
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Polymorphic variation of the guanosine triphosphate cyclohydrolase 1 gene predicts outcome in patients undergoing surgical treatment for lumbar degenerative disc disease. [electronic resource] by
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- Dai, Feng
- Belfer, Inna
- Banco, Robert J
- Martha, Julia F
- Tighiouart, Hocine
- Tromanhauser, Scott G
- Jenis, Louis G
- Hunter, David J
- Schwartz, Carolyn E
Producer: 20110802
In:
Spine vol. 35
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