例句與造句

1. These data indicate that SCN1A mutations when found contribute to a more severe clinical phenotype of Panayiotopoulos syndrome.
2. The findings resulted in Depienne et al . to identify PCDH19 mutations in patients with SCN1A negative Dravet syndrome.
3. Currently, the SCN1A gene is the most clinically relevant; the largest number of epilepsy related mutations characterized thus far occur in this gene.
4. A heterozygous inheritance of an SCN1A mutation is all that is necessary to develop a defective sodium channel; patients with Dravet syndrome will still have one normal copy of the gene.
5. Known causative genes for GEFS + are the sodium channel ? subunit genes SCN1A and SCN2A and the ? subunit gene SCN1B . Mutations in the GABA A receptor ? subunit GABRG1 are also causative for this disorder.
6. It's difficult to find scn1a in a sentence. 用scn1a造句挺難的
7. SCN1A mutations have been reported in a child and in 2 siblings with relatively early onset of seizures, prolonged time over which many seizures have occurred, and strong association of seizures with febrile precipitants even after the age of 5 years.
8. FHM3 is a rare subtype of FHM and is caused by mutations in a sodium channel ?-subunit coding gene, SCN1A . These three subtypes do not account for all cases of FHM, suggesting the existence of at least one other locus ( FHM4 ).
9. The proteins of these channels are named Na v 1.1 through Na v 1.9 . The gene names are referred to as SCN1A through SCN11A ( the SCN6 / 7A gene is part of the Na x sub-family and has uncertain function ).
10. Its cause and pathophysiology ( cause and mechanisms by which damage occurs ) are different from other epilepsies, although the symptoms are very similar to other epileptic syndromes, such as Generalized epilepsy with febrile seizures plus ( GEFS + ), Dravet syndrome with SCN1A negative, FIRES ( febrile infection related epilepsy syndrome ) Lennox-Gastaut syndrome or epilepsy of unknown origin.