Related references
Note: Only part of the references are listed.Discordant phenotypes in fraternal twins having an identical mutation in exon ORF15 of the RPGR gene
Saloni Walia et al.
ARCHIVES OF OPHTHALMOLOGY (2008)
RPGR mutation analysis and disease: An update
Xinhua Shu et al.
HUMAN MUTATION (2007)
Comprehensive survey of mutations in RP2 and RPGR in patients affected with distinct retinal dystrophies: Genotype-phenotype correlations and impact on genetic counseling
Valerie Pelletier et al.
HUMAN MUTATION (2007)
The pattern of inheritance of X-linked traits is not dominant or recessive, just X-linked
WB Dobyns
ACTA PAEDIATRICA (2006)
Dominant, gain-of-function mutant produced by truncation of RPGR
DH Hong et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2004)
Dominant X linked retinitis pigmentosa is frequently accounted for by truncating mutations in exon ORF15 of the RPGR gene
JM Rozet et al.
JOURNAL OF MEDICAL GENETICS (2002)
Share Paper
