Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency.

Kunal Ray, Moumita Chaki, Mainak Sengupta

Research output: Contribution to journalArticle

1 Citation (Scopus)
Original languageEnglish (US)
Pages (from-to)556
Number of pages1
JournalHuman Genetics
Volume122
Issue number5
StatePublished - Dec 2007

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Deficiency Diseases
Monophenol Monooxygenase
Missense Mutation
Amino Acid Substitution
Heterozygote
Codon
India
Mutation
Genes

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

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Novel human pathological mutations. Gene symbol : TYR. Disease: tyrosinase deficiency. / Ray, Kunal; Chaki, Moumita; Sengupta, Mainak.

In: Human Genetics, Vol. 122, No. 5, 12.2007, p. 556.

Research output: Contribution to journalArticle

Ray, K, Chaki, M & Sengupta, M 2007, 'Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency.', Human Genetics, vol. 122, no. 5, pp. 556.
Ray, Kunal ; Chaki, Moumita ; Sengupta, Mainak. / Novel human pathological mutations. Gene symbol : TYR. Disease: tyrosinase deficiency. In: Human Genetics. 2007 ; Vol. 122, No. 5. pp. 556.
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