Rescue From Oculocutaneous Albinism Type 4 Using Medaka slc45a2 cDNA Driven by Its Own Promoter

Patients and vertebrate mutants with oculocutaneous albinism type 4 (OCA4) have mutations in the solute carrier family 45 member 2 (slc45a2) gene. However, there is no empirical evidence for this gene–phenotype relationship. There is a unique OCA4 mutant in medaka (b) that exhibits albinism only in...

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Bibliografski detalji
Glavni autori: Fukamachi, Shoji, Kinoshita, Masato, Tsujimura, Taro, Shimada, Atsuko, Oda, Shoji, Shima, Akihiro, Meyer, Axel, Kawamura, Shoji, Mitani, Hiroshi
Format: Artigo
Jezik:Inglês
Izdano: Genetics Society of America 2008
Teme:
Investigations
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2248340/
https://ncbi.nlm.nih.gov/pubmed/18245373
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.107.073387
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