Globally,CYP1B1Mutations in Primary Congenital Glaucoma Are Strongly Structured by Geographic and Haplotype Backgrounds-Reference-Cited by-同舟云学术

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Globally,CYP1B1Mutations in Primary Congenital Glaucoma Are Strongly Structured by Geographic and Haplotype Backgrounds

Published:2006-01-01 Issue:1 Volume:47 Page:43
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Chakrabarti Subhabrata¹,Kaur Kiranpreet¹,Kaur Inderjeet¹,Mandal Anil K.²,Parikh Rajul S.³,Thomas Ravi²,Majumder Partha P.⁴

Affiliation:

1. From the Kallam Anji Reddy Molecular Genetics Laboratory, the

2. Jasti V. Ramanamma Children’s Eye Care Centre, and the3VST Centre for Glaucoma Care, L. V. Prasad Eye Institute, Hyderabad, India; and the

3. VST Centre for Glaucoma Care, L. V. Prasad Eye Institute, Hyderabad, India; and the

4. Human Genetics Unit, Indian Statistical Institute, Kolkata, India.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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1. TEK gene‐related primary congenital glaucoma: Phenotypic features and mutational spectrum in a Mexican cohort of 10 unrelated families;American Journal of Medical Genetics Part A;2024-06-07

2. Genetics and Glaucoma: the state of the art;Frontiers in Medicine;2023-12-12

3. Exome-based mutation screening in South African children with primary congenital glaucoma;Eye;2022-01-29

4. Genetics of Congenital Glaucoma;Genetics of Ocular Diseases;2022

5. Carrier Status for p.Gly61Glu and p.Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran;Journal of Ophthalmic and Vision Research;2021-10-25

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