Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556 - Concepedia

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Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556

26

Citations

36

References

2019

Year

Edmund Cauley, Ahlam A. Hamed, Inaam N. Mohamed, Maha A. Elseed, Samantha Martinez, Ashraf Yahia, Fatima Abozar, Rayan Abubakr, Mahmoud Koko, Liena E. O. Elsayed,

Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseasePathologyNeurogeneticsDisease Gene IdentificationMedicineClinical Genetics

References

	Year	Citations

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