Pages that link to "Q28261796"
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The following pages link to Farber lipogranulomatosis: clinical and molecular genetic analysis reveals a novel mutation in an Indian family (Q28261796):
Displayed 10 items.
- Population genetic analysis of the N-acylsphingosine amidohydrolase gene associated with mental activity in humans (Q24647682) (← links)
- Lysosomal storage disorders in the newborn (Q37401176) (← links)
- Accumulation of ordered ceramide-cholesterol domains in farber disease fibroblasts (Q37500658) (← links)
- Microarray analysis of the toxicogenomics and the genotoxic potential of a cationic lipid-based gene delivery nanosystem in human alveolar epithelial a549 cells (Q38514695) (← links)
- The MYH7 p.R787H mutation causes hypertrophic cardiomyopathy in two unrelated families (Q42715737) (← 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)
- Chronic lung injury and impaired pulmonary function in a mouse model of acid ceramidase deficiency (Q47372850) (← links)
- Identification of the N-acylsphingosine amidohydrolase 1 gene (ASAH1) for susceptibility to schizophrenia in a Han Chinese population. (Q51810935) (← links)
- Molecular analyses of novel ASAH1 mutations causing Farber lipogranulomatosis: analyses of exonic splicing enhancer inactivating mutation. (Q54417194) (← links)
- Acid ceramidase deficiency: Farber disease and SMA-PME (Q90370648) (← links)