Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19q.
A clinical, psychophysical, and electrophysiologic study was undertaken of two autosomal dominant retinitis pigmentosa pedigrees with a genetic mutation assigned to chromosome 19q by linkage analysis. Members with the abnormal haplotype were either symptomatic with adolescent onset nyctalopia, restr...
में बचाया:
| में प्रकाशित: | Br J Ophthalmol |
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| मुख्य लेखकों: | , , , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
BMJ Publishing Group
1995
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC505271/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7488604/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/bjo.79.9.841 |
| टैग: |
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