| Language | English |
|---|---|
| Journal | EYE |
| Volume | 25 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - 2011 |
Cite this
Chamney, S., McLoone, E., & Willoughby, C. E. (2011). A mutation in the Norrie disease gene (NDP) associated with familial exudative vitreoretinopathy. EYE, 25(12). https://doi.org/10.1038/eye.2011.226
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title = "A mutation in the Norrie disease gene (NDP) associated with familial exudative vitreoretinopathy",
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Chamney, S, McLoone, E & Willoughby, CE 2011, 'A mutation in the Norrie disease gene (NDP) associated with familial exudative vitreoretinopathy', EYE, vol. 25, no. 12. https://doi.org/10.1038/eye.2011.226
A mutation in the Norrie disease gene (NDP) associated with familial exudative vitreoretinopathy. / Chamney, S.; McLoone, E.; Willoughby, C.E.
In: EYE, Vol. 25, No. 12, 2011.Research output: Contribution to journal › Article
TY - JOUR
T1 - A mutation in the Norrie disease gene (NDP) associated with familial exudative vitreoretinopathy
AU - Chamney, S.
AU - McLoone, E.
AU - Willoughby, C.E.
N1 - Cited By :3 Export Date: 6 September 2018
PY - 2011
Y1 - 2011
U2 - 10.1038/eye.2011.226
DO - 10.1038/eye.2011.226
M3 - Article
VL - 25
JO - EYE
T2 - EYE
JF - EYE
SN - 0950-222X
IS - 12
ER -
Chamney S, McLoone E, Willoughby CE. A mutation in the Norrie disease gene (NDP) associated with familial exudative vitreoretinopathy. EYE. 2011;25(12). https://doi.org/10.1038/eye.2011.226