HBA

(redirected from SCN2A)
Also found in: Medical.

HBA

(Host Bus Adapter) See host adapter.
References in periodicals archive ?
SCN1A genindeki de novo islev kaybi mutasyonlari cogu olgudan sorumlu olmakla beraber SCN1B, SCN2A, GABRG2, GABRA1, STXBP1, PCDH19 mutasyonlari pozitif olan ya da klinik olarak Dravet Sendromu tanisi alip mutasyon saptanamayan olgular da vardir (7, 8).
Here, we reported a case of SCN2A -related seizure disorder, in which the likely pathogenic variant was only possible to be detected with the use of targeted gene panel with next-generation sequencing.
A set of RT-QuIC quadruple reactions was performed with mouse rPrP (89-231) and [PrP.sup.Sc] seeds from ScN2a cells diluted 5 x [10.sup.-4]-fold.
Sugawara et al., "A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline," Journal of Neuroscience, vol.
By decoding her genetic make-up and analysing the genes of her parents they have found she suffers from a genetic mutation of the SCN2A gene.
For instance, the previously mentioned study of 928 autism patients also highlighted two autism probands carrying nonsense de novo mutations on the SCN2A gene, which encodes a sodium channel alpha subunit; the gene previously has been shown to have strong associations with seizure disorders.
Using immortalized neuroblastoma cells ScN2a, chronically infected by the Rocky Mountain Laboratory (RML) prion strain, Naslavsky et al.
In addition, risk alterations were found in genes associated with fragile X or related syndromes (CAPRIN1 and AFF2), social-cognitive deficits (VIP), epilepsy (SCN2A and KCNQ2) as well as NRXN1 and CHD7, which causes ASD-associated CHARGE syndrome.