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The silk proteins , sericin and fibroin in silkworm , Bombyx mori
The domesticated silkworm, Bombyx mori Linn., a lepidopteran molecular model and an important economic insect that are emerging as an ideal molecular genetic resource for solving a broad range ofExpand
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Molecular basis of albinism in India: evaluation of seven potential candidate genes and some new findings.
Albinism represents a group of genetic disorders with a broad spectrum of hypopigmentary phenotypes dependent on the genetic background of the patients. Oculocutaneous albinism (OCA) patients haveExpand
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Comprehensive analysis of the molecular basis of oculocutaneous albinism in Indian patients lacking a mutation in the tyrosinase gene
Background  Oculocutaneous albinism (OCA) refers to a group of inherited disorders where the patients have little or no pigment in the eyes, skin and hair. Mutations in genes regulating multi‐stepExpand
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Functional assessment of tyrosinase variants identified in individuals with albinism is essential for unequivocal determination of genotype‐to‐phenotype correlation
Oculocutaneous albinism type 1 (OCA1), caused by pathogenic variations in the tyrosinase gene (TYR), is the most frequent and severe form of hypopigmentary disorder worldwide. While OCA1A manifestsExpand
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