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Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia. [electronic resource] by
- Farazi Fard, Mohammad Ali
- Rebelo, Adriana P
- Buglo, Elena
- Nemati, Hamid
- Dastsooz, Hassan
- Gehweiler, Ina
- Reich, Selina
- Reichbauer, Jennifer
- Quintáns, Beatriz
- Ordóñez-Ugalde, Andrés
- Cortese, Andrea
- Courel, Steve
- Abreu, Lisa
- Powell, Eric
- Danzi, Matt C
- Martuscelli, Nicole B
- Bis-Brewer, Dana M
- Tao, Feifei
- Zarei, Fariba
- Habibzadeh, Parham
- Yavarian, Majid
- Modarresi, Farzaneh
- Silawi, Mohammad
- Tabatabaei, Zahra
- Yousefi, Masoume
- Farpour, Hamid Reza
- Kessler, Christoph
- Mangold, Elisabeth
- Kobeleva, Xenia
- Tournev, Ivailo
- Chamova, Teodora
- Mueller, Amelie J
- Haack, Tobias B
- Tarnopolsky, Mark
- Gan-Or, Ziv
- Rouleau, Guy A
- Synofzik, Matthis
- Sobrido, María-Jesús
- Jordanova, Albena
- Schüle, Rebecca
- Zuchner, Stephan
- Faghihi, Mohammad Ali
Publication details: American journal of human genetics Jun 2019
In:
American journal of human genetics vol. 104
Availability: No items available.
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11.
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Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia. [electronic resource] by
- Farazi Fard, Mohammad Ali
- Rebelo, Adriana P
- Buglo, Elena
- Nemati, Hamid
- Dastsooz, Hassan
- Gehweiler, Ina
- Reich, Selina
- Reichbauer, Jennifer
- Quintáns, Beatriz
- Ordóñez-Ugalde, Andrés
- Cortese, Andrea
- Courel, Steve
- Abreu, Lisa
- Powell, Eric
- Danzi, Matt C
- Martuscelli, Nicole B
- Bis-Brewer, Dana M
- Tao, Feifei
- Zarei, Fariba
- Habibzadeh, Parham
- Yavarian, Majid
- Modarresi, Farzaneh
- Silawi, Mohammad
- Tabatabaei, Zahra
- Yousefi, Masoume
- Farpour, Hamid Reza
- Kessler, Christoph
- Mangold, Elisabeth
- Kobeleva, Xenia
- Tournev, Ivailo
- Chamova, Teodora
- Mueller, Amelie J
- Haack, Tobias B
- Tarnopolsky, Mark
- Gan-Or, Ziv
- Rouleau, Guy A
- Synofzik, Matthis
- Sobrido, María-Jesús
- Jordanova, Albena
- Schüle, Rebecca
- Zuchner, Stephan
- Faghihi, Mohammad Ali
Producer: 20200203
In:
American journal of human genetics vol. 104
Availability: No items available.
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12.
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Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model. [electronic resource] by
- Westeneng, Henk-Jan
- Debray, Thomas P A
- Visser, Anne E
- van Eijk, Ruben P A
- Rooney, James P K
- Calvo, Andrea
- Martin, Sarah
- McDermott, Christopher J
- Thompson, Alexander G
- Pinto, Susana
- Kobeleva, Xenia
- Rosenbohm, Angela
- Stubendorff, Beatrice
- Sommer, Helma
- Middelkoop, Bas M
- Dekker, Annelot M
- van Vugt, Joke J F A
- van Rheenen, Wouter
- Vajda, Alice
- Heverin, Mark
- Kazoka, Mbombe
- Hollinger, Hannah
- Gromicho, Marta
- Körner, Sonja
- Ringer, Thomas M
- Rödiger, Annekathrin
- Gunkel, Anne
- Shaw, Christopher E
- Bredenoord, Annelien L
- van Es, Michael A
- Corcia, Philippe
- Couratier, Philippe
- Weber, Markus
- Grosskreutz, Julian
- Ludolph, Albert C
- Petri, Susanne
- de Carvalho, Mamede
- Van Damme, Philip
- Talbot, Kevin
- Turner, Martin R
- Shaw, Pamela J
- Al-Chalabi, Ammar
- Chiò, Adriano
- Hardiman, Orla
- Moons, Karel G M
- Veldink, Jan H
- van den Berg, Leonard H
Producer: 20190315
In:
The Lancet. Neurology vol. 17
Availability: No items available.
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