Bardet–Biedl syndrome in two unrelated patients with identical compound heterozygous SCLT1 mutations - Concepedia

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Bardet–Biedl syndrome in two unrelated patients with identical compound heterozygous SCLT1 mutations

DOI Full Paper Access

16

Citations

16

References

2020

Year

Naoya Morisada, Riku Hamada, Kenichiro Miura, Ming Juan Ye, Kandai Nozu, Motoshi Hattori, Kazumoto Iijima

CEN Case Reports

Unrelated PatientsMendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseasePathologyBardet–biedl SyndromeMolecular GeneticsMedical GeneticsDisease Gene IdentificationMedicine

References

	Year	Citations

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