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Tyrosinase gene (TYR) mutations in Chinese patients with oculocutaneous albinism type 1

The most common mutation is a deletion that encompasses the first 10 exons of the gene along with portions of the CARKL gene upstream of CTNS

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Imaging Dynamic Neuroimmune Responses to LPS in Tobacco Smokers: A [11C]PBR28 PET Study

Maxillary sinus augmentation with a synthetic cell-binding peptide: histological and histomorphometrical results in humans