Abstract | BACKGROUND: SUBJECTS AND METHODS: Genomic DNA samples from 63 unrelated patients with autosomal dominant retinitis pigmentosa (ADRP) and 33 patients with autosomal recessive retinitis pigmentosa (ARRP) were screened by single-strand conformational polymorphism analysis followed by direct sequencing. Clinical features associated with a mutation were demonstrated by visual acuity, visual field testing, fundus photography, and electroretinography. RESULTS: A novel transitional mutation converting GGA to AGA at codon 157 (G157R) was identified. This mutation has been found in three index patients from three independent families. Phenotypic examination of seven members of the three families revealed that this mutation was associated with RP with or without macular involvement in five members, macular degeneration in one member, and asymptomatic normal phenotype in one member. In addition, previously unknown polymorphic changes including V29V, Y57Y, T87I, and L180L were identified. CONCLUSIONS: A racial difference exists in the spectrum of mutations and/or polymorphisms in the GCAP 2 gene between British and Japanese populations. Our findings suggest that the mutation in the GCAP 2 gene can cause one form of autosomal dominant retinal dystrophy, with variable phenotypic expression and incomplete penetrance.
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Authors | Motoya Sato, Mitsuru Nakazawa, Tomoaki Usui, Naoyuki Tanimoto, Haruki Abe, Hiroshi Ohguro |
Journal | Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie
(Graefes Arch Clin Exp Ophthalmol)
Vol. 243
Issue 3
Pg. 235-42
(Mar 2005)
ISSN: 0721-832X [Print] Germany |
PMID | 15452722
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Calcium-Binding Proteins
- GUCA1B protein, human
- Guanylate Cyclase-Activating Proteins
- Isoleucine
- Threonine
- Arginine
- Glycine
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Topics |
- Adult
- Aged
- Amino Acid Sequence
- Arginine
- Base Sequence
- Calcium-Binding Proteins
(genetics)
- Electroretinography
- Female
- Fundus Oculi
- Genes, Dominant
- Genetic Testing
- Glycine
- Guanylate Cyclase-Activating Proteins
- Humans
- Isoleucine
- Male
- Middle Aged
- Molecular Sequence Data
- Mutation
- Pedigree
- Retinal Diseases
(genetics, pathology, physiopathology)
- Threonine
- Visual Fields
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