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JAMA Ophthalmology, ISSN 2168-6165, 05/2015, Volume 133, Issue 5, p. 511
  Screening for splice site mutation c.828+3A>T in the peripherin 2 (PRPH2) gene should be a high priority in families with highly variable retinal... 
Genetic disorders | Genes | Eye diseases | Mutation | Ophthalmology | Polymorphism
Journal Article
JAMA Ophthalmology, ISSN 2168-6165, 07/2014, Volume 132, Issue 7, pp. 866 - 866
  X-linked retinitis pigmentosa is a severe inherited retinal degenerative disease with a frequency of 1 in 100 000 persons. Because no cure is available for... 
Clinical trials | Retina | Eye diseases | Ophthalmology | Fatty acids
Journal Article
American Journal of Ophthalmology, ISSN 0002-9394, 11/2005, Volume 140, Issue 5, p. 858
  Purpose To evaluate the clinical features associated with the RP10 form of autosomal-dominant retinitis pigmentosa in 11 affected members of various ages... 
Electrodes | Enzymes | Diabetic retinopathy | Retina | Mutation | Metabolism | Patients | Age
Journal Article
Journal Article
JAMA OPHTHALMOLOGY, ISSN 2168-6165, 08/2018, Volume 136, Issue 8, pp. 849 - 856
IMPORTANCE There are no approved drug treatments for autosomal dominant retinitis pigmentosa, a relentlessly progressive cause of adult and childhood... 
FIELD FUNDUS AUTOFLUORESCENCE | DYSTROPHY | PERIMETRY | DOCOSAHEXAENOIC ACID | OPHTHALMOLOGY | RHODOPSIN MUTATIONS | PROGRESSION | Online First | Original Investigation | Research
Journal Article
Journal Article
Investigative Opthalmology & Visual Science, ISSN 1552-5783, 02/2016, Volume 57, Issue 2, p. 349
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 10/1996, Volume 271, Issue 42, p. 26032
The interactions of reductants with dopamine β-monooxygenase (DβM) were examined using two novel classes of reductants. The steady-state kinetics of the... 
Journal Article
Journal Article
Teaching and Learning in Nursing, ISSN 1557-3087, 2007, Volume 2, Issue 4, pp. 126 - 132
The purpose of this article is to review the current literature to ascertain reasons behind parental refusal or delay of childhood immunizations. Recurring... 
Health education | Immunization | Nursing
Journal Article
American journal of ophthalmology, ISSN 0002-9394, 11/2005, Volume 140, Issue 5, pp. 858 - 867
Journal Article
01/2008, ISBN 1109023235
Usher syndrome is a genetic disease that includes visual impairment, due to progressive retinal degeneration, as well as congenital hearing loss. Night... 
Biochemistry | Public health
Dissertation
Journal Article
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