A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract.

C.E. Willoughby, S. Arab, R. Gandhi, S. Zeinali, D. Luk, G. Billingsley, F.L. Munier, E. Héon

Research output: Contribution to journalArticle

56 Citations (Scopus)
LanguageEnglish
JournalJournal of Medical Genetics
Volume40
Issue number11
Publication statusPublished - 2003

Cite this

Willoughby, C.E. ; Arab, S. ; Gandhi, R. ; Zeinali, S. ; Luk, D. ; Billingsley, G. ; Munier, F.L. ; Héon, E. / A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract. In: Journal of Medical Genetics. 2003 ; Vol. 40, No. 11.
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Willoughby, CE, Arab, S, Gandhi, R, Zeinali, S, Luk, D, Billingsley, G, Munier, FL & Héon, E 2003, 'A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract.', Journal of Medical Genetics, vol. 40, no. 11.

A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract. / Willoughby, C.E.; Arab, S.; Gandhi, R.; Zeinali, S.; Luk, D.; Billingsley, G.; Munier, F.L.; Héon, E.

In: Journal of Medical Genetics, Vol. 40, No. 11, 2003.

Research output: Contribution to journalArticle

TY - JOUR

T1 - A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract.

AU - Willoughby, C.E.

AU - Arab, S.

AU - Gandhi, R.

AU - Zeinali, S.

AU - Luk, D.

AU - Billingsley, G.

AU - Munier, F.L.

AU - Héon, E.

N1 - Cited By :54 Export Date: 6 September 2018

PY - 2003

Y1 - 2003

M3 - Article

VL - 40

JO - Journal of Medical Genetics

T2 - Journal of Medical Genetics

JF - Journal of Medical Genetics

SN - 0022-2593

IS - 11

ER -