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Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1A. [electronic resource] by
- Soldovieri, Maria Virginia
- Boutry-Kryza, Nadia
- Milh, Mathieu
- Doummar, Diane
- Heron, Benedicte
- Bourel, Emilie
- Ambrosino, Paolo
- Miceli, Francesco
- De Maria, Michela
- Dorison, Nathalie
- Auvin, Stephane
- Echenne, Bernard
- Oertel, Julie
- Riquet, Audrey
- Lambert, Laetitia
- Gerard, Marion
- Roubergue, Anne
- Calender, Alain
- Mignot, Cyril
- Taglialatela, Maurizio
- Lesca, Gaetan
Producer: 20141006
In:
Human mutation vol. 35
Availability: No items available.
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2498.
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2499.
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The F0F1 ATP Synthase Complex Localizes to Membrane Rafts in Gonadotrope Cells. [electronic resource] by
- Allen-Worthington, Krystal
- Xie, Jianjun
- Brown, Jessica L
- Edmunson, Alexa M
- Dowling, Abigail
- Navratil, Amy M
- Scavelli, Kurt
- Yoon, Hojean
- Kim, Do-Geun
- Bynoe, Margaret S
- Clarke, Iain
- Roberson, Mark S
Producer: 20171227
In:
Molecular endocrinology (Baltimore, Md.) vol. 30
Availability: No items available.
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