About: Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores.

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About: Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores. Goto Sponge NotDistinct Permalink

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Author	Lunardi, Joël (1950-.... ; auteur en biologie) Marty, Isabelle (19..-.... ; biologiste) Fauré, Julien (19..-.... ; biologiste) Ferreiro, Ana (19..-....) Sacconi, Sabrina (1972-....) Desnuelle, Claude (1947-.... ; neurologue)
Bibliographic Citation	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. Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores.. Human Mutation, Wiley, 2008, 29 (5), pp.670-8. ⟨10.1002/humu.20696⟩ 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. Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores.. Human Mutation, 2008, 29 (5), pp.670-8. ⟨10.1002/humu.20696⟩
Title	Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores.
dc:date	2008
Digital Object Identifier (DOI)	10.1002/humu.20696

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