Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa - Concepedia

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Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa

DOI Full Paper Access

36

Citations

23

References

2016

Year

Andrea Angius, Paolo Uva, Insa Buers, Manuela Oppo, Alessandro Puddu, Stefano Onano, Ivana Persico, Angela Loi, Loredana Marcia, Wolfgang Höhne,

The American Journal of Human Genetics

Bi-allelic MutationsEarly-onset Retinitis PigmentosaAllelic VariantGenetic DisorderGeneticsMolecular GeneticsDisease Gene IdentificationKlhl7 CauseMedicineCell Biology

References

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