Molecular basis of type I (tryrosinase-related) oculocutaneous albinism: Mutations and polymorphisms of the human tyrosinase gene
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference41 articles.
1. Human tyrosinase gene, mapped to chromosome 11 (q14 → q21), defines second region of homology with mouse chromosome 7
2. Expression of the mouse tyrosinase gene during embryonic development: recapitulation of the temporal regulation in transgenic mice.
3. A single base insertion in the putative transmembrane domain of the tyrosinase gene as a cause for tyrosinase-negative oculocutaneous albinism.
4. RFLP for Mbol in the human tyrosinase (TYR) gene detected by PCR
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