Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome - Concepedia

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Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome

DOI Full Paper Access

132

Citations

34

References

2014

Year

Estelle Colin, Evelyne Huynh Cong, Géraldine Mollet, Agnès Guichet, Olivier Gribouval, Christelle Arrondel, Olivia Boyer, Laurent Daniel, Marie-Claire Gübler, Zelal Ekinci,

The American Journal of Human Genetics

Galloway-mowat SyndromeDisease MechanismGenetic DisorderMedicineGeneticsInherited Metabolic DiseasePathogenesisRenal PathologyPathologyImmunologySteroid-resistant Nephrotic SyndromeDisease Gene IdentificationChronic Kidney DiseaseWdr73 Are Responsible

References

	Year	Citations

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