(Q52533780)
Statements
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). (English)
Hodes ME
Zimmerman AW
Aydanian A
Naidu S
Miller NR
Garcia Oller JL
Barker B
Aleck KA
Hurley TD
Dlouhy SR
1 January 1999
82
2
132-139