Literature DB >> 1348580

An MboI polymorphism at codon 192 of the human tyrosinase gene is present in Asians and Afrocaribbeans.

J D Johnston1, A F Winder, L H Breimer.   

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Year:  1992        PMID： 1348580      PMCID： PMC312212          DOI： 10.1093/nar/20.6.1433

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  3 in total

1.  Detection of mutations in the tyrosinase gene in a patient with type IA oculocutaneous albinism.

Authors:  R A Spritz; K M Strunk; L B Giebel; R A King
Journal:  N Engl J Med       Date:  1990-06-14       Impact factor: 91.245

2.  Non-random distribution of missense mutations within the human tyrosinase gene in type I (tyrosinase-related) oculocutaneous albinism.

Authors:  R A King; M M Mentink; W S Oetting
Journal:  Mol Biol Med       Date:  1991-02

3.  RFLP for MboI in the human tyrosinase (TYR) gene detected by PCR.

Authors:  L B Giebel; R A Spritz
Journal:  Nucleic Acids Res       Date:  1990-05-25       Impact factor: 16.971
  3 in total
  1 in total

1.  A frequent tyrosinase gene mutation associated with type I-A (tyrosinase-negative) oculocutaneous albinism in Puerto Rico.

Authors:  W S Oetting; C J Witkop; S A Brown; R Colomer; J P Fryer; K E Bloom; R A King
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025
  1 in total

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