Disruption of the ATP8A2 gene in a patient with a t(10;13) de novo balanced translocation and a severe neurological phenotype - Concepedia

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Disruption of the ATP8A2 gene in a patient with a t(10;13) de novo balanced translocation and a severe neurological phenotype

DOI Full Paper Access

140

Citations

5

References

2010

Year

Pierre Cacciagli, Marie-Reine Haddad, Cécile Mignon‐Ravix, Bilal El Waly, Anne Moncla, Chantal Missirian, B. Chabrol, Laurent Villard

European Journal of Human Genetics

Severe Neurological PhenotypeGenetic DisorderGeneticsMolecular GeneticsMolecular NeurobiologyAtp8a2 GeneMedicineCell BiologyNeurogenetics

References

	Year	Citations

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