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- [7] A newly discovered LGI1 mutation in Korean family with autosomal dominant lateral temporal lobe epilepsy [J]. SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2014, 23 (01): : 69 - 73
- [10] Whole exome sequencing identifies a novel NRL mutation in a Chinese family with autosomal dominant retinitis pigmentosa [J]. MOLECULAR VISION, 2016, 22 : 234 - 242