Novel human pathological mutations. Gene symbol: TYR. Disease: albinism, oculocutaneous 1.

Kunal Ray, Moumita Chaki, Mainak Sengupta

Research output: Contribution to journalArticle

Original languageEnglish (US)
Pages (from-to)555
Number of pages1
JournalHuman Genetics
Volume122
Issue number5
StatePublished - Dec 2007

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Oculocutaneous Albinism
Monophenol Monooxygenase
Missense Mutation
Amino Acid Substitution
Heterozygote
Codon
India
Mutation
Genes
Oculocutaneous albinism type 1

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

Novel human pathological mutations. Gene symbol : TYR. Disease: albinism, oculocutaneous 1. / Ray, Kunal; Chaki, Moumita; Sengupta, Mainak.

In: Human Genetics, Vol. 122, No. 5, 12.2007, p. 555.

Research output: Contribution to journalArticle

Ray, Kunal ; Chaki, Moumita ; Sengupta, Mainak. / Novel human pathological mutations. Gene symbol : TYR. Disease: albinism, oculocutaneous 1. In: Human Genetics. 2007 ; Vol. 122, No. 5. pp. 555.
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