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A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3.

Genetic loci for X-linked retinitis pigmentosa (XLRP) have been mapped between Xp11.22 and Xp22.13 (RP2, RP3, RP6, and RP15). The RP3 gene, which is responsible for the predominant form of XLRP in most Caucasian populations, has been localized to Xp21.1 by linkage analysis and the map positions of c...

詳細記述

保存先:
書誌詳細
主要な著者: Fujita, R., Bingham, E., Forsythe, P., McHenry, C., Aita, V., Navia, B. A., Dry, K., Segal, M., Devoto, M., Bruns, G., Wright, A. F., Ott, J., Sieving, P. A., Swaroop, A.
フォーマット: Artigo
言語:Inglês
出版事項: 1996
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC1915116/
https://ncbi.nlm.nih.gov/pubmed/8659520
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