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Analysis of the RPGRGene in 11 Pedigrees with the Retinitis Pigmentosa Type 3 Genotype: Paucity of Mutations in the Coding Region but Splice Defects in Two Families

✍ Scribed by Ricardo Fujita; Monika Buraczynska; Linn Gieser; Weiping Wu; Patricia Forsythe; Magnus Abrahamson; Samuel G. Jacobson; Paul A. Sieving; Sten Andréasson; Anand Swaroop


Book ID
117855175
Publisher
American Society of Human Genetics
Year
1997
Tongue
English
Weight
513 KB
Volume
61
Category
Article
ISSN
0002-9297

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