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RP2 and RPGR Mutations and Clinical Correlations in Patients with X-Linked Retinitis Pigmentosa

โœ Scribed by Dror Sharon; Michael A. Sandberg; Vivian W. Rabe; Melissa Stillberger; Thaddeus P. Dryja; Eliot L. Berson


Book ID
117854328
Publisher
American Society of Human Genetics
Year
2003
Tongue
English
Weight
426 KB
Volume
73
Category
Article
ISSN
0002-9297

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โœ Maria Guevara-Fujita; Stacey Fahrner; Kinga Buraczynska; Jason Cook; Dianna Whea ๐Ÿ“‚ Article ๐Ÿ“… 2001 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 24 KB ๐Ÿ‘ 2 views

X-linked forms of retinitis pigmentosa (XLRP) are among the most severe because of their early onset, often leading to significant visual impairment before the fourth decade. RP3, genetically localized at Xp21.1, accounts for 70% of XLRP in different populations. The RPGR (Retinitis Pigmentosa GTPas