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Publications by S S Dandekar

An Atypical Phenotype of Macular and Peripapillary Retinal Atrophy Caused by a Mutation in the RP2 Gene

British Journal of Ophthalmology

Molecular Neuroscience

Sensory Systems

English

Related publications

Phenotype of Three Consanguineous Tunisian Families With Early-Onset Retinal Degeneration Caused by an R91W Homozygous Mutation in the RPE65 Gene

Graefe's Archive for Clinical and Experimental Ophthalmology

Molecular Neuroscience

Sensory Systems

English

The Delayed Terminal Flower Phenotype Is Caused by a Conditional Mutation in the CENTRORADIALIS Gene of Snapdragon

Plant Physiology

English

Peripapillary Atrophy in Stargardt Disease

English

4H Leukodystrophy Caused by a Homozygous POLR3B Mutation: Further Delineation of the Phenotype

American Journal of Medical Genetics, Part A

English

Association of Retinal and Macular Damage With Brain Atrophy in Multiple Sclerosis

Multidisciplinary

English

P496 X- Linked Infantile Spinal Muscular Atrophy (Smax2) Caused by Novel C.1681g>a Substitution in the Uba1 Gene, Expanding the Phenotype

English

Topographic Localization of Macular Retinal Ganglion Cell Loss Associated With Localized Peripapillary Retinal Nerve Fiber Layer Defect

Investigative Ophthalmology and Visual Science

Molecular Neuroscience

Sensory Systems

English

A Phenotype of Atypical Apraxia of Speech in a Family Carrying SQSTM1 Mutation

Journal of Alzheimer's Disease

Clinical Psychology

English

Keratoendotheliitis Fugax Hereditaria Is Caused by a Mutation in the NLRP3 Gene

Acta Ophthalmologica

English