PLP1
proteolipid protein 1
Ассоциированные заболевания
Герминативная мутация (причина)7
Pelizaeus-Merzbacher disease, connatal formORPHA:280210
→Pelizaeus-Merzbacher disease, classic formORPHA:280219
→Null syndromeORPHA:280234
→Pelizaeus-Merzbacher disease, transitional formORPHA:280224
→Pelizaeus-Merzbacher disease in female carriersORPHA:280229
→Hypomyelination of early myelinating structuresORPHA:599376
→Spastic paraplegia type 2ORPHA:99015
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