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Business Profiles

Researchgate: Elise Héon

Toronto, Ontario, Canada

Private Homepages

New Study on Promise of Gene Therapy for Leber Congenital Amaurosis

www.elsevier.com

Novel Therapy for Blindness Works Only When Specific Gene Mutation Present

Scientific Publications

Eight previously unidentified mutations found in the OA1 ocular...

bmcmedgenet.biomedcentral.com

BMC Medical Genetics. Volume 7; Viewing options. Abstract; Full text; ... Alex V Levin, Elise Héon, Joanne Sutherland, Didier Lacombe, Edith Said, Eedy Mezer, ...

Publications

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Autosomal Recessive Retinitis Pigmentosa Caused by Mutations in the...

core.ac.uk

By Edwin M. Stone, Xunda Luo, Elise Héon, Byron L. Lam, Richard G. Weleber, Jennifer A. Halder, Louisa M. Affatigato, Jacqueline B. Goldberg, Alexander Sumaroka ...

Defining the Pathogenicity of Optineurin in Juvenile Open-Angle...

core.ac.uk

By Colin E. Willoughby, Louie Loh Yen Chan, Sarah Herd, Gail Billingsley, Nima Noordeh, Alex V. Levin, Yvonne Buys, Graham Trope, Mansoor Sarfarazi and Elise Héon

Values of electroretinogram responses according to axial length |...

link.springer.com

M. Panton; Dayle Sigesmund; Alex V. Levin; Ken K. Nischal; Elise Héon.

core.ac.uk

By S. Mohsen Hosseini, Sarah Herd, Andrea L. Vincent and Elise Héon. Abstract. Genetic analysis of chromosome 20-related posterior polymorphous corneal …

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Facebook: Elise Heon | Facebook

LinkedIn: elise heon - Physician - The Hospital for Sick …

LinkedIn: Elise Heon - Canada | LinkedIn

LinkedIn: Elise Heon | LinkedIn

Business Profiles

Researchgate: Elise Héon

Private Homepages

New Study on Promise of Gene Therapy for Leber Congenital Amaurosis

Related Documents

Elise Héon - Academia.edu

Scientific Publications

Eight previously unidentified mutations found in the OA1 ocular...

Publications

Autosomal Recessive Retinitis Pigmentosa Caused by Mutations in the...

Defining the Pathogenicity of Optineurin in Juvenile Open-Angle...

Values of electroretinogram responses according to axial length |...

©2008 Molecular Vision - CORE

Miscellaneous

Avery's Journey

CRYBA4, a Novel Human Cataract Gene, Is Also Involved in...

(PDF) Ocular Genetics Program: multidisciplinary care of patients...

Dr Jenea Bin | The University of Edinburgh

Phenotypic heterogeneity of CYP1B1: Mutations in a patient with...

Phenotypic Characterization of La Plaine Retinal Degeneration | EVRS