Publication | Closed Access
Molecular basis of acid ceramidase deficiency in a neonatal form of Farber disease: Identification of the first large deletion in ASAH1 gene
30
Citations
26
References
2013
Year
Acid Ceramidase DeficiencyGenetic DisorderGeneticsPathogenesisInherited Metabolic DiseasePathologyMolecular GeneticsDisease Gene IdentificationAsah1 GeneMedicineFarber DiseaseOxidative Stress
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