Clinical Heterogeneity in a Family With Mutations in USH2A
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| Veröffentlicht in: | JAMA ophthalmology 2015-03, Vol.133 (3), p.352 |
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| container_issue | 3 |
| container_start_page | 352 |
| container_title | JAMA ophthalmology |
| container_volume | 133 |
| creator | Lenassi, Eva Robson, Anthony G Luxon, Linda M Bitner-Glindzicz, Maria Webster, Andrew R |
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| doi_str_mv | 10.1001/jamaophthalmol.2014.5163 |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 2168-6165 |
| ispartof | JAMA ophthalmology, 2015-03, Vol.133 (3), p.352 |
| issn | 2168-6165 2168-6173 |
| language | eng |
| recordid | cdi_crossref_primary_10_1001_jamaophthalmol_2014_5163 |
| source | MEDLINE; American Medical Association Journals |
| subjects | Adult Deafness - genetics DNA Mutational Analysis Electroretinography Exons - genetics Extracellular Matrix Proteins - genetics Female Genetic Heterogeneity Humans Male Middle Aged Mutation Retinitis Pigmentosa - genetics Siblings Usher Syndromes - genetics |
| title | Clinical Heterogeneity in a Family With Mutations in USH2A |
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