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

Carol L. Freund; Qing Liang Wang; Shiming Chen; Brenda L. Muskat; Carmella D. Wiles; Val C. Sheffield; Samuel G. Jacobson; Roderick R. McLnnes; Donald J. Zack; Edwin M. Stone

doi:10.1038/ng0498-311

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

Carol L. Freund, Qing Liang Wang, Shiming Chen, Brenda L. Muskat, Carmella D. Wiles, Val C. Sheffield, Samuel G. Jacobson, Roderick R. McLnnes, Donald J. Zack, Edwin M. Stone

Research output: Contribution to journal › Letter › peer-review

263 Scopus citations

Original language	English
Pages (from-to)	311-312
Number of pages	2
Journal	Nature Genetics
Volume	18
Issue number	4
DOIs	https://doi.org/10.1038/ng0498-311
State	Published - Apr 1998

Access to Document

10.1038/ng0498-311

Cite this

@article{87551bc21fc34329b5f1dec45a167036,

title = "De novo mutations in the CRX homeobox gene associated with leber congenital amaurosis",

author = "Freund, {Carol L.} and Wang, {Qing Liang} and Shiming Chen and Muskat, {Brenda L.} and Wiles, {Carmella D.} and Sheffield, {Val C.} and Jacobson, {Samuel G.} and McLnnes, {Roderick R.} and Zack, {Donald J.} and Stone, {Edwin M.}",

year = "1998",

month = apr,

doi = "10.1038/ng0498-311",

language = "English",

volume = "18",

pages = "311--312",

journal = "Nature Genetics",

issn = "1061-4036",

number = "4",

}

TY - JOUR

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

AU - Freund, Carol L.

AU - Wang, Qing Liang

AU - Chen, Shiming

AU - Muskat, Brenda L.

AU - Wiles, Carmella D.

AU - Sheffield, Val C.

AU - Jacobson, Samuel G.

AU - McLnnes, Roderick R.

AU - Zack, Donald J.

AU - Stone, Edwin M.

PY - 1998/4

Y1 - 1998/4

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

U2 - 10.1038/ng0498-311

DO - 10.1038/ng0498-311

M3 - Letter

C2 - 9537410

AN - SCOPUS:0032037626

SN - 1061-4036

VL - 18

SP - 311

EP - 312

JO - Nature Genetics

JF - Nature Genetics

IS - 4

ER -

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

Access to Document

Other files and links

Cite this