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)

M. E. Hodes, Andrew W. Zimmerman, Antonina Aydanian, Sakkubai Naidu, Neil R. Miller, José L. Garcia Oller, Bruce Barker, Kirk A. Aleck, Thomas D. Hurley, Stephen R. Dlouhy

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