Results
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3821.
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3822.
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3823.
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3824.
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3825.
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3826.
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3827.
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3828.
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3829.
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3830.
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3831.
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3832.
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3833.
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An X-linked channelopathy with cardiomegaly due to a CLIC2 mutation enhancing ryanodine receptor channel activity. [electronic resource] by
- Takano, Kyoko
- Liu, Dan
- Tarpey, Patrick
- Gallant, Esther
- Lam, Alex
- Witham, Shawn
- Alexov, Emil
- Chaubey, Alka
- Stevenson, Roger E
- Schwartz, Charles E
- Board, Philip G
- Dulhunty, Angela F
Producer: 20130621
In:
Human molecular genetics vol. 21
Availability: No items available.
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3834.
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3835.
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A novel late-onset axial myopathy associated with mutations in the skeletal muscle ryanodine receptor (RYR1) gene. [electronic resource] by
- Løseth, Sissel
- Voermans, Nicol C
- Torbergsen, Torberg
- Lillis, Sue
- Jonsrud, Christoffer
- Lindal, Sigurd
- Kamsteeg, Erik-Jan
- Lammens, Martin
- Broman, Marcus
- Dekomien, Gabriele
- Maddison, Paul
- Muntoni, Francesco
- Sewry, Caroline
- Radunovic, Aleksandar
- de Visser, Marianne
- Straub, Volker
- van Engelen, Baziel
- Jungbluth, Heinz
Producer: 20140115
In:
Journal of neurology vol. 260
Availability: No items available.
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3836.
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3837.
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3838.
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3839.
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3840.
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