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1 Ergebnisse
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Expanding the clinical-pathological and genetic spectrum of..:
Fusto A
;
Cassandrini D
;
Fiorillo C
...
info:eu-repo/semantics/altIdentifier/pmid/35428369. , 2022
Link:
https://hdl.handle.net/2434/925384
RT Journal T1
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study
UL https://suche.suub.uni-bremen.de/peid=base-ftunivmilanoair:oai:air.unimi.it:2434_925384&Exemplar=1&LAN=DE A1 Fusto A A1 Cassandrini D A1 Fiorillo C A1 Codemo V A1 Astrea G A1 D'Amico A A1 Maggi L A1 Magri F A1 Pane M A1 Tasca G A1 Sabbatini D A1 Bello L A1 Battini R A1 Bernasconi P A1 Fattori F A1 Bertini E. S A1 Comi G A1 Messina S A1 Mongini T A1 Moroni I A1 Panicucci C A1 Berardinelli A A1 Donati A A1 Nigro V A1 Pini A A1 Giannotta M A1 Dosi C A1 Ricci E A1 Mercuri E A1 Minervini G A1 Tosatto S A1 Santorelli F A1 Bruno C A1 Pegoraro E PB BioMed Central YR 2022 K1 Central core disease K1 Genotype–phenotype correlation K1 Multi-minicore disease K1 Neuromuscular disorder K1 Protein modelling K1 RYR1-related myopathie K1 Human K1 Muscle K1 Skeletal K1 Mutation K1 Ryanodine Receptor Calcium Release Channel K1 Myopathies K1 Structural K1 Congenital K1 Myopathy K1 Central Core K1 Settore MED/26 - Neurologia JF info:eu-repo/semantics/altIdentifier/pmid/35428369 LK http://dx.doi.org/https://hdl.handle.net/2434/925384 DO https://hdl.handle.net/2434/925384 SF ELIB - SuUB Bremen
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