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- [22] Identification and functional study of novel PLP1 mutations in Chinese patients with Pelizaeus-Merzbacher disease BRAIN & DEVELOPMENT, 2015, 37 (08): : 797 - 802
- [30] Deep intronic deletion in intron 3 of PLP1 is associated with a severe phenotype of Pelizaeus-Merzbacher disease Human Genome Variation, 8