OBJECTIVE: The present study aims to investigate the gene mutations of CHRNB2, CHRNA2 and CHRNA4 in Chinese population with autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE). METHODS: 257 ADNFLE patients (74 sporadic and 32 familial) were collected, including 42 pedigree patients and 215 sporadic cases. Exon mutational screening of CHRNB2, CHRNA2 and CHRNA4 was performed by direct PCR sequencing. RESULTS: No published mutations of CHRNB2, CHRNA4 and CHRNA2 genes were detected in this study. Three kinds of c.SNP (c.66C> T, c.249C> T, c.375A> G) were detected on the 2(nd) and 5(th) exons of CHRNA2; six kinds of c.SNP (c.639T> C, c.678T> C, c.1209G> T, c.1227T> C, c.1659G> A, c.1629C> T) were detected on the 5(th) exon of CHRNA4. Three novel mutations were discovered, respectively locating on the exon 5 of CHRNA4 gene (c.570C> T), 5(th) and 6(th) exons of CHRNB2 gene (c.483C> T and c.1407C> G). The three mutations were absent in 200 healthy controls, indicating that the mutations were very rare. CONCLUSION: CHRNA4, CHRNB2 and CHRNA2 may be not the causative genes of Chinese ADNFLE population. Whether the three novel synonymous mutations were genetic factors of ADNFLE pathogenesis in Chinese Han population needs to be further studied.
OBJECTIVE: The present study aims to investigate the gene mutations of CHRNB2, CHRNA2 and CHRNA4 in Chinese population with autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE). METHODS: 257 ADNFLE patients (74 sporadic and 32 familial) were collected, including 42 pedigree patients and 215 sporadic cases. Exon mutational screening of CHRNB2, CHRNA2 and CHRNA4 was performed by direct PCR sequencing. RESULTS: No published mutations of CHRNB2, CHRNA4 and CHRNA2 genes were detected in this study. Three kinds of c.SNP (c.66C> T, c.249C> T, c.375A> G) were detected on the 2(nd) and 5(th) exons of CHRNA2; six kinds of c.SNP (c.639T> C, c.678T> C, c.1209G> T, c.1227T> C, c.1659G> A, c.1629C> T) were detected on the 5(th) exon of CHRNA4. Three novel mutations were discovered, respectively locating on the exon 5 of CHRNA4 gene (c.570C> T), 5(th) and 6(th) exons of CHRNB2 gene (c.483C> T and c.1407C> G). The three mutations were absent in 200 healthy controls, indicating that the mutations were very rare. CONCLUSION:CHRNA4, CHRNB2 and CHRNA2 may be not the causative genes of Chinese ADNFLE population. Whether the three novel synonymous mutations were genetic factors of ADNFLE pathogenesis in Chinese Han population needs to be further studied.
Authors: Ailsa McLellan; Hilary A Phillips; Christopher Rittey; Martin Kirkpatrick; John C Mulley; David Goudie; John B P Stephenson; John Tolmie; Ingrid E Scheffer; Samuel F Berkovic; Sameer M Zuberi Journal: Epilepsia Date: 2003-04 Impact factor: 5.864
Authors: Jean-Charles Hoda; Wenli Gu; Marc Friedli; Hilary A Phillips; Sonia Bertrand; Stylianos E Antonarakis; David Goudie; Richard Roberts; Ingrid E Scheffer; Carla Marini; Jayesh Patel; Samuel F Berkovic; John C Mulley; Ortrud K Steinlein; Daniel Bertrand Journal: Mol Pharmacol Date: 2008-05-02 Impact factor: 4.436
Authors: O K Steinlein; J C Mulley; P Propping; R H Wallace; H A Phillips; G R Sutherland; I E Scheffer; S F Berkovic Journal: Nat Genet Date: 1995-10 Impact factor: 38.330