Determination of variants in the 3′-region of the Tyrosinase gene requires locus specific amplification
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference28 articles.
1. Identification and Characterization of a DNase Hypersensitive Region of the Human Tyrosinase Gene
2. A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism.
3. Organization and nucleotide sequences of the human tyrosinase gene and a truncated tyrosinase-related segment
4. A tyrosinase gene missense mutation in temperature-sensitive type I oculocutaneous albinism. A human homologue to the Siamese cat and the Himalayan mouse.
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1. Oculocutaneous Albinism (OCA) Type 1–5;Genetic Syndromes;2024
2. Evidence that the Ser192Tyr/Arg402Gln in cis Tyrosinase gene haplotype is a disease-causing allele in oculocutaneous albinism type 1B (OCA1B);npj Genomic Medicine;2022-01-13
3. Non-syndromic Oculocutaneous Albinism: Novel Genetic Variants and Clinical Follow Up of a Brazilian Pediatric Cohort;Frontiers in Genetics;2020-04-28
4. Identification of a functionally significant tri-allelic genotype in the Tyrosinase gene (TYR) causing hypomorphic oculocutaneous albinism (OCA1B);Scientific Reports;2017-06-30
5. Delineating the genetic heterogeneity of OCA in Hungarian patients;European Journal of Medical Research;2017-06-19
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