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Erratum to: Intragenic polymorphic missense mutations in theXLRS1gene in families with juvenile X-linked retinoschisis

โœ Scribed by Miki Hiraoka; Michael T. Trese; Barkur S. Shastry


Publisher
Springer
Year
1999
Tongue
English
Weight
11 KB
Volume
105
Category
Article
ISSN
0340-6717

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โœ Yukihiko Mashima; Kei Shinoda; Susumu Ishida; Yoko Ozawa; Jun Kudoh; Takeshi Iwa ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 21 KB ๐Ÿ‘ 2 views

The XLRS1 gene (HUGO-approved symbol, RS1) has been found to cause X-linked recessive retinoschisis (RS) which is characterized by splitting of the superficial layer of the retina. Recent mutation analysis of this gene revealed 82 different mutations in 214 patients with RS. We have now identified 1