Chelsea S Norman
1PUBLICATIONS
7CO-AUTHORS

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Publications (1)
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|Jan 14, 2022
Evidence that the Ser192Tyr/Arg402Gln in cis Tyrosinase gene haplotype is a disease-causing allele in oculocutaneous albinism type 1B (OCA1B).Siying Lin, Aida Sanchez-Bretaño, Joseph S Leslie
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