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

K. Ray, Moumita Chaki, Arijit Mukhopadhyay

Research output: Contribution to journalArticle

Original languageEnglish (US)
Pages (from-to)299
Number of pages1
JournalHuman Genetics
Volume117
Issue number2-3
StatePublished - Jul 2005

Fingerprint

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

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

Ray, K., Chaki, M., & Mukhopadhyay, A. (2005). Gene symbol: TYR. Disease: Albinism, oculocutaneous 1. Human Genetics, 117(2-3), 299.

Gene symbol : TYR. Disease: Albinism, oculocutaneous 1. / Ray, K.; Chaki, Moumita; Mukhopadhyay, Arijit.

In: Human Genetics, Vol. 117, No. 2-3, 07.2005, p. 299.

Research output: Contribution to journalArticle

Ray, K, Chaki, M & Mukhopadhyay, A 2005, 'Gene symbol: TYR. Disease: Albinism, oculocutaneous 1.', Human Genetics, vol. 117, no. 2-3, pp. 299.
Ray K, Chaki M, Mukhopadhyay A. Gene symbol: TYR. Disease: Albinism, oculocutaneous 1. Human Genetics. 2005 Jul;117(2-3):299.
Ray, K. ; Chaki, Moumita ; Mukhopadhyay, Arijit. / Gene symbol : TYR. Disease: Albinism, oculocutaneous 1. In: Human Genetics. 2005 ; Vol. 117, No. 2-3. pp. 299.
@article{d8869eb2faab48468ecdabebd6f0732e,
title = "Gene symbol: TYR. Disease: Albinism, oculocutaneous 1.",
author = "K. Ray and Moumita Chaki and Arijit Mukhopadhyay",
year = "2005",
month = "7",
language = "English (US)",
volume = "117",
pages = "299",
journal = "Human Genetics",
issn = "0340-6717",
publisher = "Springer Verlag",
number = "2-3",

}

TY - JOUR

T1 - Gene symbol

T2 - TYR. Disease: Albinism, oculocutaneous 1.

AU - Ray, K.

AU - Chaki, Moumita

AU - Mukhopadhyay, Arijit

PY - 2005/7

Y1 - 2005/7

UR - http://www.scopus.com/inward/record.url?scp=26944491543&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=26944491543&partnerID=8YFLogxK

M3 - Article

C2 - 16156027

AN - SCOPUS:26944491543

VL - 117

SP - 299

JO - Human Genetics

JF - Human Genetics

SN - 0340-6717

IS - 2-3

ER -