Bibliografia UJ CM

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Arnaud Blanchard, Agathe Roubertie, Marion Simonetta-Moreau, Vuthy Ea, Coline Coquart, Melissa Y. Frederic, Gael Gallouedec, Jean-Paul Adenis, Isabelle Benatru, Michel Borg, Pierre Burbaud, Patrick Calvas, Laura Cif, Philippe Damier, Alain Destee, Laurence Faivre, Lucie Guyant-Marechal, Piotr Janik, Samer Janoura, Alexandre Kreisler, Anna Lusakowska, Sylvie Odent, Anna Potulska-Chromik, Monika Rudzińska, Stephane Thobois, Isabelle Vuillaume, Christine Tranchant, Sylvie Tuffery-Giraud, Philippe Coubes, Bernard Sablonniere, Mireille Claustres, Gwenaelle Collod-Beroud.
Singular DYT6 phenotypes in association with new THAP1 frameshift mutations.
Movement Disorders
2011 : Vol. 26, nr 9, s. 1775-1777, bibliogr. 8 poz.
p-ISSN: 0885-3185
LR
AIF
IF: 4.505
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Marie-Christine Chartier-Harlin, Justus C. Dachsel, Carles Vilarino-Guell, Sarah J. Lincoln, Frederic Lepretre, Mary M. Hulihan, Jennifer Kachergus, Austen J. Milnerwood, Lucia Tapia, Mee-Sook Song, Emilie Le Rhun, Eugenie Mutez, Lydie Larvor, Aurelie Duflot, Christel Vanbesien-Mailliot, Alexandre Kreisler, Owen A. Ross, Kenya Nishioka, Alexandra I. Soto-Ortolaza, Stephanie A. Cobb, Heather A. Melrose, Bahareh Behrouz, Brett H. Keeling, Justin A. Bacon, Emna Hentati, Lindsey Williams, Akiko Yanagiya, Nahum Sonenberg, Paul J. Lockhart, Abba C. Zubair, Ryan J. Uitti, Jan O. Aasly, Anna Krygowska-Wajs, Grzegorz Opala, Zbigniew K. Wszolek, Roberta Frigerio, Demetrius M. Maraganore, David Gosal, Tim Lynch, Michael Hutchinson, Anna Rita Bentivoglio, Enza Maria Valente, William C. Nichols, Nathan Pankratz, Tatiana Foroud, Rachel A. Gibson, Faycal Hentati, Dennis W. Dickson, Alain Destee, Matthew J. Farrer.
Translation initiator EIF4G1 mutations in familial Parkinson disease.
American Journal of Human Genetics
2011 : Vol. 89, nr 3, s. 398-406, bibliogr. 25 poz.
p-ISSN: 0002-9297
AZ
ORG
AIF
IF: 10.603
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