Limbal stem cell deficiency and ocular phenotype in ectrodactyly-ectodermal dysplasia-clefting syndrome caused by p63 mutations

E. Di Iorio; S.B. Kaye; D. Ponzin; V. Barbaro; S. Ferrari; E. Böhm; P. Nardiello; G. Castaldo; J.A. McGrath; C.E. Willoughby

doi:10.1016/j.ophtha.2011.06.044

Limbal stem cell deficiency and ocular phenotype in ectrodactyly-ectodermal dysplasia-clefting syndrome caused by p63 mutations

E. Di Iorio, S.B. Kaye, D. Ponzin, V. Barbaro, S. Ferrari, E. Böhm, P. Nardiello, G. Castaldo, J.A. McGrath, C.E. Willoughby

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

96 Citations (Scopus)

Original language	English
Pages (from-to)	74-83
Number of pages	10
Journal	Ophthalmology: Journal of the American Academy of Ophthalmology
Volume	119
Issue number	1
DOIs	https://doi.org/10.1016/j.ophtha.2011.06.044
Publication status	Published (in print/issue) - 2012

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Cited By :34

Export Date: 6 September 2018

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10.1016/j.ophtha.2011.06.044

https://www.scopus.com/inward/record.uri?eid=2-s2.0-84555161203&doi=10.1016%2fj.ophtha.2011.06.044&partnerID=40&md5=41e9ab3395008ade72f06fcbabc88fed

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Di Iorio, E., Kaye, S. B., Ponzin, D., Barbaro, V., Ferrari, S., Böhm, E., Nardiello, P., Castaldo, G., McGrath, J. A., & Willoughby, C. E. (2012). Limbal stem cell deficiency and ocular phenotype in ectrodactyly-ectodermal dysplasia-clefting syndrome caused by p63 mutations. Ophthalmology: Journal of the American Academy of Ophthalmology, 119(1), 74-83. https://doi.org/10.1016/j.ophtha.2011.06.044

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Di Iorio, E, Kaye, SB, Ponzin, D, Barbaro, V, Ferrari, S, Böhm, E, Nardiello, P, Castaldo, G, McGrath, JA & Willoughby, CE 2012, 'Limbal stem cell deficiency and ocular phenotype in ectrodactyly-ectodermal dysplasia-clefting syndrome caused by p63 mutations', Ophthalmology: Journal of the American Academy of Ophthalmology, vol. 119, no. 1, pp. 74-83. https://doi.org/10.1016/j.ophtha.2011.06.044

TY - JOUR

T1 - Limbal stem cell deficiency and ocular phenotype in ectrodactyly-ectodermal dysplasia-clefting syndrome caused by p63 mutations

AU - Di Iorio, E.

AU - Kaye, S.B.

AU - Ponzin, D.

AU - Barbaro, V.

AU - Ferrari, S.

AU - Böhm, E.

AU - Nardiello, P.

AU - Castaldo, G.

AU - McGrath, J.A.

AU - Willoughby, C.E.

N1 - Cited By :34 Export Date: 6 September 2018

PY - 2012

Y1 - 2012

UR - https://www.scopus.com/pages/publications/84555161203

U2 - 10.1016/j.ophtha.2011.06.044

DO - 10.1016/j.ophtha.2011.06.044

M3 - Article

SN - 1549-4713

VL - 119

SP - 74

EP - 83

JO - Ophthalmology: Journal of the American Academy of Ophthalmology

JF - Ophthalmology: Journal of the American Academy of Ophthalmology

IS - 1

ER -

Limbal stem cell deficiency and ocular phenotype in ectrodactyly-ectodermal dysplasia-clefting syndrome caused by p63 mutations

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