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PedAM

Pediatric Disease Annotations & Medicines




Disease lateral sclerosis
Phenotype C1848954|generalized dystonia
Sentences 1
PubMedID- 24562058 Objective: to determine the genetic etiology in 2 consanguineous families who presented a novel phenotype of autosomal recessive juvenile amyotrophic lateral sclerosis associated with generalized dystonia.

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