Publication | Open Access
Whole-Exome Sequencing Links a Variant in DHDDS to Retinitis Pigmentosa
172
Citations
12
References
2011
Year
Functional GenomicsMendelian DisorderGenetic DisorderNext-generation SequencingGeneticsPathologyMolecular GeneticsWhole-exome Sequencing LinksDisease Gene IdentificationGenomicsMedicineBioinformaticsVariant Interpretation
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