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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)
Hodes, M.E., Zimmerman, Andrew W., Aydanian, Antonina, Naidu, Sakkubai, Miller, Neil R., Oller, Jos� L. Garcia, Barker, Bruce, Aleck, Kirk A., Hurley, Thomas D., Dlouhy, Stephen R.Volume:
82
Language:
english
Pages:
8
Journal:
American Journal of Medical Genetics
DOI:
10.1002/(sici)1096-8628(19990115)82:23.0.co;2-4
Date:
January, 1999
File:
PDF, 530 KB
english, 1999