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PedAM

Pediatric Disease Annotations & Medicines




Disease spastic paraparesis
Phenotype C0023520|leukodystrophy
Sentences 1
PubMedID- 21366909 Fa2h-deficiency was identified as the cause of a new leukodystrophy with spastic paraparesis [16], and hereditary spastic paraplegia spg35 [17], respectively.

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