Heterozygous FOXC1 Mutation (M161K) Associated with Congenital Glaucoma and Aniridia in an Infant and a Milder Phenotype in Her Mother (vol 29, pg 67, 2008)

Journal article

Peer reviewed

Arif O. Khan, Mohammad A. Aldahmesh and Abdullah Al-Amri

Ophthalmic genetics, Vol.29(4), pp.190-190

01/12/2008

Abstract

Genetics & Heredity

Life Sciences & Biomedicine

Ophthalmology

Science & Technology

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Title: Heterozygous FOXC1 Mutation (M161K) Associated with Congenital Glaucoma and Aniridia in an Infant and a Milder Phenotype in Her Mother (vol 29, pg 67, 2008)
Creators - without role: Arif O. Khan - King Khalid Eye Specialist Hosp, Pediat Ophthalmol Div, Riyadh 11462, Saudi Arabia
Mohammad A. Aldahmesh - King Faisal Specialist Hosp & Res Ctr, Arabian Diagnost Labs, Riyadh 11211, Saudi Arabia
Abdullah Al-Amri - EMERGENCY
Publication Details: Ophthalmic genetics, Vol.29(4), pp.190-190
Publisher: Taylor & Francis
Number of pages: 1
Identifiers: 9933010408331
Academic Unit: University of Jeddah
Language: English
Resource Type: Journal article