Pages that link to "Q50571349"
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The following pages link to Farber lipogranulomatosis type 1--late presentation and early death in a Croatian boy with a novel homozygous ASAH1 mutation. (Q50571349):
Displayed 6 items.
- Acid ceramidase treatment enhances the outcome of autologous chondrocyte implantation in a rat osteochondral defect model. (Q36706155) (← links)
- Systemic ceramide accumulation leads to severe and varied pathological consequences. (Q37188558) (← links)
- Molecular basis of acid ceramidase deficiency in a neonatal form of Farber disease: identification of the first large deletion in ASAH1 gene (Q44533383) (← links)
- Atypical presentation of infantile-onset farber disease with novel ASAH1 mutations. (Q52127961) (← links)
- Acid Ceramidase Deficiency in Mice Leads to Severe Ocular Pathology and Visual Impairment (Q64042504) (← links)
- Acid ceramidase deficiency: Farber disease and SMA-PME (Q90370648) (← links)