Endoplasmic reticulum retention is a common defect associated with tyrosinase-negative albinism
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference52 articles.
1. Molecular basis of albinism: Mutations and polymorphisms of pigmentation genes associated with albinism
2. MAMMALIAN TYROSINASE: PREPARATION AND PROPERTIES
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4. Mutational mapping of the catalytic activities of human tyrosinase.
5. Isolation and sequence of a cDNA clone for human tyrosinase that maps at the mouse c-albino locus.
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