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- Q91103843 description "artículu científicu espublizáu en xineru de 2019" @default.
- Q91103843 description "im Januar 2019 veröffentlichter wissenschaftlicher Artikel" @default.
- Q91103843 description "scientific article published on 17 January 2019" @default.
- Q91103843 description "wetenschappelijk artikel" @default.
- Q91103843 description "наукова стаття, опублікована 17 січня 2019" @default.
- Q91103843 name "Mutations in ACTL6B, coding for a subunit of the neuron-specific chromatin remodeling complex nBAF, cause early onset severe developmental and epileptic encephalopathy with brain hypomyelination and cerebellar atrophy" @default.
- Q91103843 name "Mutations in ACTL6B, coding for a subunit of the neuron-specific chromatin remodeling complex nBAF, cause early onset severe developmental and epileptic encephalopathy with brain hypomyelination and cerebellar atrophy" @default.
- Q91103843 type Item @default.
- Q91103843 label "Mutations in ACTL6B, coding for a subunit of the neuron-specific chromatin remodeling complex nBAF, cause early onset severe developmental and epileptic encephalopathy with brain hypomyelination and cerebellar atrophy" @default.
- Q91103843 label "Mutations in ACTL6B, coding for a subunit of the neuron-specific chromatin remodeling complex nBAF, cause early onset severe developmental and epileptic encephalopathy with brain hypomyelination and cerebellar atrophy" @default.
- Q91103843 prefLabel "Mutations in ACTL6B, coding for a subunit of the neuron-specific chromatin remodeling complex nBAF, cause early onset severe developmental and epileptic encephalopathy with brain hypomyelination and cerebellar atrophy" @default.
- Q91103843 prefLabel "Mutations in ACTL6B, coding for a subunit of the neuron-specific chromatin remodeling complex nBAF, cause early onset severe developmental and epileptic encephalopathy with brain hypomyelination and cerebellar atrophy" @default.
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- Q91103843 P698 Q91103843-68AB5B5F-F119-4974-AA6A-F27B60BCBBEB @default.
- Q91103843 P356 S00439-019-01972-3 @default.
- Q91103843 P698 30656450 @default.
- Q91103843 P1433 Q5937167 @default.
- Q91103843 P1476 "Mutations in ACTL6B, coding for a subunit of the neuron-specific chromatin remodeling complex nBAF, cause early onset severe developmental and epileptic encephalopathy with brain hypomyelination and cerebellar atrophy" @default.
- Q91103843 P2093 "Eliana Salvo" @default.
- Q91103843 P2093 "Martina Miceli" @default.
- Q91103843 P2093 "Maurizio Elia" @default.
- Q91103843 P304 "187-198" @default.
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- Q91103843 P356 "10.1007/S00439-019-01972-3" @default.
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- Q91103843 P577 "2019-01-17T00:00:00Z" @default.
- Q91103843 P698 "30656450" @default.