Farber disease is an extremely rare autosomal recessive lysosomal storage disease marked by “Farber lipogranulomatosis: clinical and molecular genetic analysis reveals a novel mutation in
Benz[b]indeno[2,1-e]pyran,dione 1a and analogues have been prepared and studied for enhancing the biosynthesis of erythropoietin. The scope of the Baker–Venkataraman rearrangement is illustrated by way
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Gleichenia linearis (Burm. f.) C.B. Clarke Show All Show Tabs. General Information. Symbol: GLLI3. Group: Fern. Family: Gleicheniaceae. Duration. Gleichenia linearis (Burm. f.) C.B. Clarke.
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