7Chen S, Song C, Guo H, et al. Distinct novel mutations affecting the same base in the NIPA1 gene cause autosomal dominant hereditary spastic paraplegia in two Chinese families. Hum Murat, 2005, 25: 135-141. 被引量：1
8Reed JA, Wilkinson PA, Patel H, et al. A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia. Neurogenetics, 2005, 6: 79-84. 被引量：1
9Goytain A, Hines RM, El-Husseini A, et al. NIPA1 ( SPG6 ), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg^2+ transporter. J Biol Chem, 2007, 282 : 8060-8068. 被引量：1
10Windpassinger C, Auer-Grumbach M, Irobi J, et al. Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome. Nat Genet, 2004, 36: 271-276. 被引量：1
