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Segawa syndrome due to mutation Q89X in the GCH1 gene: a possible founder effect in Córdoba (southern Spain). [electronic resource] by
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- Ochoa-Sepúlveda, Juan José
- Ochoa-Amor, Juan José
- Bescansa-Heredero, Enrique
- Camino-León, Rafael
- Gascón-Jiménez, Francisco Javier
- Mateos-González, Maria Elena
- Pérez-Navero, Juan Luis
- Lao-Villadóniga, José Ignacio
- Ormazabal, Aida
- Artuch, Rafael
- Beyer, Katrin
Producer: 20100101
In:
Journal of neurology vol. 256
Availability: No items available.
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Parkinson's disease in GTP cyclohydrolase 1 mutation carriers. [electronic resource] by
- Mencacci, Niccolò E
- Isaias, Ioannis U
- Reich, Martin M
- Ganos, Christos
- Plagnol, Vincent
- Polke, James M
- Bras, Jose
- Hersheson, Joshua
- Stamelou, Maria
- Pittman, Alan M
- Noyce, Alastair J
- Mok, Kin Y
- Opladen, Thomas
- Kunstmann, Erdmute
- Hodecker, Sybille
- Münchau, Alexander
- Volkmann, Jens
- Samnick, Samuel
- Sidle, Katie
- Nanji, Tina
- Sweeney, Mary G
- Houlden, Henry
- Batla, Amit
- Zecchinelli, Anna L
- Pezzoli, Gianni
- Marotta, Giorgio
- Lees, Andrew
- Alegria, Paulo
- Krack, Paul
- Cormier-Dequaire, Florence
- Lesage, Suzanne
- Brice, Alexis
- Heutink, Peter
- Gasser, Thomas
- Lubbe, Steven J
- Morris, Huw R
- Taba, Pille
- Koks, Sulev
- Majounie, Elisa
- Raphael Gibbs, J
- Singleton, Andrew
- Hardy, John
- Klebe, Stephan
- Bhatia, Kailash P
- Wood, Nicholas W
Producer: 20141106
In:
Brain : a journal of neurology vol. 137
Availability: No items available.
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640.
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