๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Two novel point mutations of the XLRS1 gene in patients with X-linked juvenile retinoschisis

โœ Scribed by Yumiko Inoue; Shuji Yamamoto; Tomoyuki Inoue; Takashi Fujikado; Shunji Kusaka; Nobuyuki Ohguro; Masahito Ohji; Yasuo Tano


Book ID
117018480
Publisher
Elsevier Science
Year
2002
Tongue
English
Weight
209 KB
Volume
134
Category
Article
ISSN
0002-9394

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Identification of four novel mutations o
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