Whole Exome Sequencing Identifies CRB1 Defect in an Unusual Maculopathy Phenotype - Concepedia

Concepedia

Publication | Open Access

Whole Exome Sequencing Identifies CRB1 Defect in an Unusual Maculopathy Phenotype

DOI Full Paper Access

69

Citations

30

References

2014

Year

Stephen H. Tsang, Tomas R. Burke, Maris Oll, Suzanne Yzer, Winston Lee, Ya‐Jing Xie, Rando Allikmets

Mendelian DisorderGenetic DisorderMedicineGeneticsPathologyUnusual Maculopathy PhenotypeMolecular GeneticsDisease Gene IdentificationMolecular DiagnosticsBioinformatics

References

	Year	Citations

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