1Clinical standards and interpretation of gene sequence variants in human Mendelian disordersTANG Bei-sha, ZENG Sheng, LI KaiSpecial Topic471-4762Strategies and problems of genetic diagnosis for neurogenetic diseasesLI Xun-hua, CHEN Ding-bang, WU ChaoSpecial Review477-4833Recent study on primary familial brain calcificationCHEN You, CEN Zhi-dong, LUO WeiSpecial Review484-4894Genetic research advance on neurodegeneration with brain iron accumulationHUANG Xiao-jun, CAO LiSpecial Review490-4995Application of gene detection in precision medicine of cerebrovascular diseaseZHE Xiao, DENG Yan-chunSpecial Review500-5066Clinical phenotype analysis of paroxysmal kinesigenic dyskinesiaTIAN Wo-tu, HUANG Xiao-jun, SHEN Jun-yi, XU Yang-qi, CHEN Sheng-di, CAO LiNeurogenetic Disorders507-5127Clinical phenotype and genetic mutation of one case with head tremor and cerebellar atrophyXIE Kun-ming, GU Wei-hong, HAO Ying, CHEN Yuan-yuan, ZHANG Jin, ZHANG XinNeurogenetic Disorders513-5188Clinical phenotype and genetic characteristics of ataxia-telangiectasia: four cases reportZHENG Lan, LIU Xiao-li, CAO LiNeurogenetic Disorders519-5259Analysis of clinical phenotype and genetic mutation with outcome evaluation in one family of vitamin B12-dependent methylmalonic aciduriaLI Jing, SUN Yi-ming, OU Li-yu, ZHU Yu-ling, WANG Liang, LI Huan, ZHANG ChengNeurogenetic Disorders526-53310Clinical phenotype and genetic mutation of fatty acid hydroxylase-associated neurodegeneration: analysis of four casesHUANG Xiao-jun, LIU Xiao-li, WANG Tian, SHEN Jun-yi, CHEN Sheng-di, TANG Wei-guo, CAO LiNeurogenetic Disorders534-54011Advances in research of invasion and recurrence of pituitary adenomaYAN Xiao-ling, ZHANG Xue-binReview541-54512Paroxysmal limb weakness for ten yearsZHANG Meng-yu, XU Yan, SHEN Jian-zhong, YANG Yin-chang, PENG Bin, CUI Li-yingClinicopathologic Discussion546-54913@@476,489,499,506,512,525,550-555