Results
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A c.3216_3217delGA mutation in AGL gene in Tunisian patients with a glycogen storage disease type III: evidence of a founder effect. [electronic resource] by
- Mili, A
- Ben Charfeddine, I
- Amara, A
- Mamaï, O
- Adala, L
- Ben Lazreg, T
- Bouguila, J
- Saad, A
- Limem, K
- Gribaa, M
Producer: 20130412
In:
Clinical genetics vol. 82
Availability: No items available.
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12128.
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12134.
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12135.
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LOPED study: looking for an early diagnosis in a late-onset Pompe disease high-risk population. [electronic resource] by
- Musumeci, O
- la Marca, G
- Spada, M
- Mondello, S
- Danesino, C
- Comi, G P
- Pegoraro, E
- Antonini, G
- Marrosu, G
- Liguori, R
- Morandi, L
- Moggio, M
- Massa, R
- Ravaglia, S
- Di Muzio, A
- Filosto, M
- Tonin, P
- Di Iorio, G
- Servidei, S
- Siciliano, G
- Angelini, C
- Mongini, T
- Toscano, A
Producer: 20160418
In:
Journal of neurology, neurosurgery, and psychiatry vol. 87
Availability: No items available.
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12136.
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NS1643 interacts around L529 of hERG to alter voltage sensor movement on the path to activation. [electronic resource] by
- Guo, Jiqing
- Cheng, Yen May
- Lees-Miller, James P
- Perissinotti, Laura L
- Claydon, Tom W
- Hull, Christina M
- Thouta, Samrat
- Roach, Daniel E
- Durdagi, Serdar
- Noskov, Sergei Y
- Duff, Henry J
Producer: 20160505
In:
Biophysical journal vol. 108
Availability: No items available.
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