Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two families (Q24678278)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two families |
scientific article |
Statements
Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two families (English)
M Buraczynska
L Gieser
W Wu
P Forsythe
M Abrahamson
S G Jacobson
P A Sieving
S Andréasson
1 September 1997
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