SciELO - Scientific Electronic Library Online

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  • Hodes ME, Zimmerman AW, Aydanian A, Naidu S, Miller NR, Garc?a Oller JL. Different mutations in the same codon of the proteolipid protein gene, PLP, may help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2). Am J Med Genet 1999;82(2):132-9.
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