Gene symbol: TYR. Disease: albinism, oculocutaneous 1.

K. Ray, Moumita Chaki, Mainak Sengupta

Research output: Contribution to journalArticle

Original languageEnglish (US)
Pages (from-to)675
Number of pages1
JournalHuman Genetics
Volume119
Issue number6
StatePublished - Jul 2006

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Oculocutaneous Albinism
Nonsense Codon
Amino Acid Substitution
Point Mutation
Genes
Oculocutaneous albinism type 1

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

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Ray, K., Chaki, M., & Sengupta, M. (2006). Gene symbol: TYR. Disease: albinism, oculocutaneous 1. Human Genetics, 119(6), 675.

Gene symbol : TYR. Disease: albinism, oculocutaneous 1. / Ray, K.; Chaki, Moumita; Sengupta, Mainak.

In: Human Genetics, Vol. 119, No. 6, 07.2006, p. 675.

Research output: Contribution to journalArticle

Ray, K, Chaki, M & Sengupta, M 2006, 'Gene symbol: TYR. Disease: albinism, oculocutaneous 1.', Human Genetics, vol. 119, no. 6, pp. 675.
Ray K, Chaki M, Sengupta M. Gene symbol: TYR. Disease: albinism, oculocutaneous 1. Human Genetics. 2006 Jul;119(6):675.
Ray, K. ; Chaki, Moumita ; Sengupta, Mainak. / Gene symbol : TYR. Disease: albinism, oculocutaneous 1. In: Human Genetics. 2006 ; Vol. 119, No. 6. pp. 675.
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