Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case report - Concepedia

Concepedia

Publication | Open Access

Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case report

DOI Full Paper Access

18

Citations

22

References

2019

Year

Rita Maria Alves, Paolo Uva, Marielza Veiga, Manuela Oppo, Fabiana C. R. Zschaber, Giampiero Porcu, Henrique P. Porto, Ivana Persico, Stefano Onano, Gianmauro Cuccuru,

BMC Medical Genetics

References

	Year	Citations

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