Functional analyses of mutant recessive GUCY2D alleles identified in Leber congenital amaurosis patients: protein domain comparisons and dominant negative effects.

No abstract is available for this paper.

• Publication year

  2004

• Venue

  Molecular Vision

• Publication date

  2004-04-20

• Fields of study

  Biology, Medicine

• Identifiers
  PMID 15123990
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Gene expression phenotype in heterozygous carriers of ataxia telangiectasia.

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• Functional consequences of a rod outer segment membrane guanylate cyclase (ROS-GC1) gene mutation linked with Leber's congenital amaurosis.

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• Primary Structure and Differential Gene Expression of Three Membrane Forms of Guanylyl Cyclase Found in the Eye of the TeleostOryzias latipes *

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• The Membrane Guanylyl Cyclase, Retinal Guanylyl Cyclase-1, Is Activated through Its Intracellular Domain (*)

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