Publication | Open Access
A Comprehensive Mutation Analysis of RP2 and RPGR in a North American Cohort of Families with X-Linked Retinitis Pigmentosa
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Citations
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References
2002
Year
North American CohortMendelian DisorderGenetic DisorderMedicineGeneticsGenetic EpidemiologyPathologyComprehensive Mutation AnalysisMolecular GeneticsDisease Gene IdentificationX-linked Retinitis PigmentosaMolecular DiagnosticsClinical Genetics
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