ERG Findings in Two Patients with Autosomal Dominant Congenital Stationary Night Blindness and His258Asn Mutation of the β-Subunit of Rod Photoreceptor CGMP-Specific Phosphodiesterase

Rosenberg, Thomas; Gal, Andreas; Simonsen, Svend Erik

doi:10.1007/978-1-4615-1897-6_42

Degenerative Diseases of the Retina 1995

DOI: 10.1007/978-1-4615-1897-6_42

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ERG Findings in Two Patients with Autosomal Dominant Congenital Stationary Night Blindness and His258Asn Mutation of the β-Subunit of Rod Photoreceptor CGMP-Specific Phosphodiesterase

Thomas Rosenberg¹,

Andreas Gal

Svend Erik Simonsen³

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1995

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ERG Findings in Two Patients with Autosomal Dominant Congenital Stationary Night Blindness and His258Asn Mutation of the β-Subunit of Rod Photoreceptor CGMP-Specific Phosphodiesterase

Cited by 1 publication

References 14 publications

Mutations in the Gene for the B-Subunit of Rod Photoreceptor Cgmp-Specific Phosphodiesterase (PDEB) in Patients with Retinal Dystrophies and Dysfunctions

Mutations in the Gene for the B-Subunit of Rod Photoreceptor Cgmp-Specific Phosphodiesterase (PDEB) in Patients with Retinal Dystrophies and Dysfunctions

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