Some Characteristics of the Electroretinogram in Hereditary Retinal Pigmentary Dystrophy. I. The Correlation of Recordability by Single Stimulus and Mode of Inheritance

Author:

Ohba N.,Tanino T.,Omoto K.

Publisher

Springer Netherlands

Reference6 articles.

1. Botermans, C. H. G.: Primary pigmentary retinal degeneration and its association with neurological diseases. In: Handbook of Clinical Neurology, vol. 13: 148–379. North-Holland Publ. Co., Amsterdam, (1972).

2. Franceschctti, A., François, J. & Babel, J.: Chorioretinal Heredodegenerations, pp. 176–180. Charles C. Thomas, Springfield, (1974).

3. Imaizumi, K.: Elcctrophysiological study of retinitis pigmentosa. Acta Soc. Ophthal.mol. Jap., 73, 2347–2487, (1969).

4. Krill, A. E. & Iser, G.: The value of electroretinography in the diagnosis of pigmentary degenerations of the retina. Amer. J. Ophthalmol., 47, 649–656, (1959).

5. Ohba, N., Tanino, T. & Omoto, K.: this proceeding.

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