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Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy. [electronic resource] by
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- Lin, Ling
- Schormair, Barbara
- Kornum, Birgitte R
- Faraco, Juliette
- Plazzi, Giuseppe
- Melberg, Atle
- Cornelio, Ferdinando
- Urban, Alexander E
- Pizza, Fabio
- Poli, Francesca
- Grubert, Fabian
- Wieland, Thomas
- Graf, Elisabeth
- Hallmayer, Joachim
- Strom, Tim M
- Mignot, Emmanuel
Producer: 20120913
In:
Human molecular genetics vol. 21
Availability: No items available.
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2584.
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Narcolepsy is a common phenotype in HSAN IE and ADCA-DN. [electronic resource] by
- Moghadam, Keivan Kaveh
- Pizza, Fabio
- La Morgia, Chiara
- Franceschini, Christian
- Tonon, Caterina
- Lodi, Raffaele
- Barboni, Piero
- Seri, Marco
- Ferrari, Simona
- Liguori, Rocco
- Donadio, Vincenzo
- Parchi, Piero
- Cornelio, Ferdinando
- Inzitari, Domenico
- Mignarri, Andrea
- Capocchi, Giuseppe
- Dotti, Maria Teresa
- Winkelmann, Juliane
- Lin, Ling
- Mignot, Emmanuel
- Carelli, Valerio
- Plazzi, Giuseppe
Producer: 20140826
In:
Brain : a journal of neurology vol. 137
Availability: No items available.
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2585.
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Histamine H3 receptor antagonists: from target identification to drug leads. [electronic resource] by
- Bonaventure, P
- Letavic, M
- Dugovic, C
- Wilson, S
- Aluisio, L
- Pudiak, C
- Lord, B
- Mazur, C
- Kamme, F
- Nishino, S
- Carruthers, N
- Lovenberg, T
Producer: 20070531
In:
Biochemical pharmacology vol. 73
Availability: No items available.
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2597.
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