New SMARCA2 mutation in a patient with Nicolaides-Baraitser syndrome and myoclonic astatic epilepsy.
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Chromatin Remodeling BAF (SWI/SNF) Complexes in Neural Development and Disorders.A SMARCA2 Mutation in the First Case Report of Nicolaides-Baraitser Syndrome in Latin America: Genotype-Phenotype CorrelationPrevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability.
P2860
New SMARCA2 mutation in a patient with Nicolaides-Baraitser syndrome and myoclonic astatic epilepsy.
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New SMARCA2 mutation in a pati ...... nd myoclonic astatic epilepsy.
@en
New SMARCA2 mutation in a pati ...... nd myoclonic astatic epilepsy.
@nl
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New SMARCA2 mutation in a pati ...... nd myoclonic astatic epilepsy.
@en
New SMARCA2 mutation in a pati ...... nd myoclonic astatic epilepsy.
@nl
prefLabel
New SMARCA2 mutation in a pati ...... nd myoclonic astatic epilepsy.
@en
New SMARCA2 mutation in a pati ...... nd myoclonic astatic epilepsy.
@nl
P2093
P2860
P356
P1476
New SMARCA2 mutation in a pati ...... nd myoclonic astatic epilepsy.
@en
P2093
EuroEPINOMICS RES myoclonic astatic epilepsy working group
K Lascelles
M A Simpson
P2860
P304
P356
10.1002/AJMG.A.37935
P407
P577
2016-09-26T00:00:00Z