Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum - Concepedia

Concepedia

Publication | Open Access

Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum

DOI Full Paper Access

31

Citations

25

References

2020

Year

Roser Urreizti, Estrella López‐Martín, Antonio Federico Martínez‐Monseny, Montse Pujadas, Laura Castilla‐Vallmanya, Luis A. Pérez‐Jurado, Mercedes Serrano, Daniel Natera‐de Benito, Beatriz Martı́nez-Delgado, Manuel Posada de la Paz,

Orphanet Journal of Rare Diseases

References

	Year	Citations

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