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Start Over Author "Escamilla Honrubia, Juan M" Publisher oxford university press / usa
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1. ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism.

Author

Panza, Emanuele, Escamilla-Honrubia, Juan M., Marco-Marín, Clara, Gougeard, Nadine, De Michele, Giuseppe, Morra, Vincenzo Brescia, Liguori, Rocco, Salviati, Leonardo, Donati, Maria Alice, Cusano, Roberto, Pippucci, Tommaso, Ravazzolo, Roberto, Németh, Andrea H., Smithson, Sarah, Davies, Sally, Hurst, Jane A., Bordo, Domenico, Rubio, Vicente, Seri, Marco, and Coutelier, Marie

Subjects
*LETTERS to the editor, *GENETIC mutation, *SPASTIC paralysis, *ACTIVITIES of daily living, *HUMAN genetics, *AMINO acid metabolism, *AMINO acids, *OXIDOREDUCTASES, *FAMILIAL spastic paraplegia
Published
2016
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