Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores. (Q46769258)
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scientific article published in May 2008
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English | Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores. |
scientific article published in May 2008 |
Statements
Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores (English)
Nicole Monnier
Isabelle Marty
Claude Desnuelle
Brigitte Estournet
Ana Ferreiro
Norma Romero
Annie Laquerriere
Leila Lazaro
Jean-Jacques Martin
Eva Morava
Annick Rossi
Anneke Van der Kooi
Marianne de Visser
Corien Verschuuren
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