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High carriers frequency of an apparently ancient founder mutation p.Tyr322X in the ERCC8 gene responsible for Cockayne syndrome among Christian Arabs in Northern Israel

✍ Scribed by Morad Khayat; Hagar Hardouf; Joel Zlotogora; Stavit Allon Shalev


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
89 KB
Volume
152A
Category
Article
ISSN
1552-4825

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