Publication | Closed Access
Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7)☆
105
Citations
43
References
2003
Year
Developmental BiologyGenetic DisorderMedicineGeneticsDegenerative DiseaseMolecular GeneticsAlternative SplicingGenomic OrganisationDisease Gene IdentificationGene ExpressionHuman Rim1Splicing Variant
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