De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis.

C. L. Freund, Q. L. Wang, S. Chen, B. L. Muskat, C. D. Wiles, V. C. Sheffield, S. G. Jacobson, R. R. McInnes, Donald J Zack, E. M. Stone

Research output: Contribution to journalArticle

Original languageEnglish (US)
Pages (from-to)311-312
Number of pages2
JournalNature Genetics
Volume18
Issue number4
StatePublished - Apr 1998

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

Freund, C. L., Wang, Q. L., Chen, S., Muskat, B. L., Wiles, C. D., Sheffield, V. C., ... Stone, E. M. (1998). De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis. Nature Genetics, 18(4), 311-312.

De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis. / Freund, C. L.; Wang, Q. L.; Chen, S.; Muskat, B. L.; Wiles, C. D.; Sheffield, V. C.; Jacobson, S. G.; McInnes, R. R.; Zack, Donald J; Stone, E. M.

In: Nature Genetics, Vol. 18, No. 4, 04.1998, p. 311-312.

Research output: Contribution to journalArticle

Freund, CL, Wang, QL, Chen, S, Muskat, BL, Wiles, CD, Sheffield, VC, Jacobson, SG, McInnes, RR, Zack, DJ & Stone, EM 1998, 'De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis.', Nature Genetics, vol. 18, no. 4, pp. 311-312.
Freund CL, Wang QL, Chen S, Muskat BL, Wiles CD, Sheffield VC et al. De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis. Nature Genetics. 1998 Apr;18(4):311-312.
Freund, C. L. ; Wang, Q. L. ; Chen, S. ; Muskat, B. L. ; Wiles, C. D. ; Sheffield, V. C. ; Jacobson, S. G. ; McInnes, R. R. ; Zack, Donald J ; Stone, E. M. / De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis. In: Nature Genetics. 1998 ; Vol. 18, No. 4. pp. 311-312.
@article{cdc71482c5fc46c0865e40ab3c1a9ec1,
title = "De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis.",
author = "Freund, {C. L.} and Wang, {Q. L.} and S. Chen and Muskat, {B. L.} and Wiles, {C. D.} and Sheffield, {V. C.} and Jacobson, {S. G.} and McInnes, {R. R.} and Zack, {Donald J} and Stone, {E. M.}",
year = "1998",
month = "4",
language = "English (US)",
volume = "18",
pages = "311--312",
journal = "Nature Genetics",
issn = "1061-4036",
publisher = "Nature Publishing Group",
number = "4",

}

TY - JOUR

T1 - De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis.

AU - Freund, C. L.

AU - Wang, Q. L.

AU - Chen, S.

AU - Muskat, B. L.

AU - Wiles, C. D.

AU - Sheffield, V. C.

AU - Jacobson, S. G.

AU - McInnes, R. R.

AU - Zack, Donald J

AU - Stone, E. M.

PY - 1998/4

Y1 - 1998/4

UR - http://www.scopus.com/inward/record.url?scp=0032037626&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0032037626&partnerID=8YFLogxK

M3 - Article

VL - 18

SP - 311

EP - 312

JO - Nature Genetics

JF - Nature Genetics

SN - 1061-4036

IS - 4

ER -