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Pelizaeus-Merzbacher disease: Cellular hypersensitivity to ultraviolet light

✍ Scribed by Sugita, Katsuo; Ishii, Mitsuko; Takanashi, Jun-ichi; Suzuki, Nobuo; Isogai, Eriko; Niimi, Hiroo


Book ID
123153412
Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
535 KB
Volume
14
Category
Article
ISSN
0387-7604

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## Abstract The __rumpshaker__ mutation of the X‐linked myelin proteolipid protein (__PLP1__) gene causes spastic paraplegia type 2 or a mild form of Pelizaeus‐Merzbacher disease in man. The identical mutation occurs spontaneously in mice. Both human and murine diseases are associated with dysmyeli