Results
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1081.
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1082.
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1083.
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1084.
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1085.
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1086.
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1087.
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1088.
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1089.
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1090.
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1091.
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1092.
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Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores. [electronic resource] by
- Monnier, Nicole
- Marty, Isabelle
- Faure, Julien
- Castiglioni, Claudia
- Desnuelle, Claude
- Sacconi, Sabrina
- Estournet, Brigitte
- Ferreiro, Ana
- Romero, Norma
- Laquerriere, Annie
- Lazaro, Leila
- Martin, Jean-Jacques
- Morava, Eva
- Rossi, Annick
- Van der Kooi, Anneke
- de Visser, Marianne
- Verschuuren, Corien
- Lunardi, Joël
Producer: 20080821
In:
Human mutation vol. 29
Availability: No items available.
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1093.
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1094.
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1095.
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1096.
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1097.
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1098.
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1099.
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1100.
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