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ARVO Annual Meeting Abstract July 2018

Mutations in IMPG1 cause autosomal dominant and recessive retinitis pigmentosa

Gael Manes; Xavier ZANLONGHI; Carmen Ayuso; Graeme Black; Guillaume OLIVIER; Béatrice Bocquet; Audrey Sénéchal; Isabelle Meunier; Christian Hamel

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):2322.

ARVO Annual Meeting Abstract April 2009

Prevalence of Mutations in BEST1 Gene in a Cohort of Patients With Presumed Best Disease

I. A. Meunier; G. Manes; B. Bocquet; C. Arndt; C. Hamel; A. Sénéchal

Invest. Ophthalmol. Vis. Sci.. 2009; 50(13):2810.

ARVO Annual Meeting Abstract May 2008

Three Families With Best’s Disease and Normal Electro-Oculogram Recordings

C. F. Arndt; I. Meunier; S. Ben Salah; C. Bazalgette; L. Valette; E. Mazoir; A. Sénéchal; C. Hamel

Invest. Ophthalmol. Vis. Sci.. 2008; 49(13):2972.

ARVO Annual Meeting Abstract May 2007

Kcnv2 Mutations in Cone Dystrophy With Supernormal Rod Electroretinogram

A. Senechal; S. Ben Salah; S. Kamei; G. Humbert; B. Arnaud; X. Zanlonghi; C. P. Hamel

Invest. Ophthalmol. Vis. Sci.. 2007; 48(13):1658.

ARVO Annual Meeting Abstract May 2004

New loci for autosomal recessive retinitis pigmentosa and macular degeneration

C. Maubaret; A. Senechal; G. Humbert; B. Arnaud; O. Rebollo; W. Kharrat; D. Hillaire; C.P. Hamel

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):4745.

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