Gene symbol: CRB1. Disease: Leber congenital amaurosis. Accession #Hm0540
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| Veröffentlicht in: | Human genetics 2006-02, Vol.118 (6), p.778-778 |
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| container_end_page | 778 |
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| container_issue | 6 |
| container_start_page | 778 |
| container_title | Human genetics |
| container_volume | 118 |
| creator | Vallespin, E Cantalapiedra, D Garcia-Hoyos, M Riveiro, R Queipo, A Trujillo-Tiebas, M J Ayuso, C |
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| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 0340-6717 |
| ispartof | Human genetics, 2006-02, Vol.118 (6), p.778-778 |
| issn | 0340-6717 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_68306161 |
| source | MEDLINE; SpringerLink Journals - AutoHoldings |
| subjects | Amino Acid Substitution Eye Proteins - genetics Humans Membrane Proteins - genetics Mutation, Missense Nerve Tissue Proteins - genetics Optic Atrophy, Hereditary, Leber - genetics |
| title | Gene symbol: CRB1. Disease: Leber congenital amaurosis. Accession #Hm0540 |
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