Novel mutations of ABCA1 transporter in patients with Tangier disease and familial HDL deficiency - Concepedia

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Novel mutations of ABCA1 transporter in patients with Tangier disease and familial HDL deficiency

DOI Full Paper Access

32

Citations

22

References

2012

Year

Tommaso Fasano, Paolo Zanoni, Claudio Rabacchi, Livia Pisciotta, Elda Favari, Maria Pia Adorni, Patrick Deegan, Adrian Park, Thinn Hlaing, Michael Feher,

Molecular Genetics and Metabolism

Mendelian DisorderDisease MechanismAbca1 TransporterGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic EpidemiologyNovel MutationsPathologyTangier DiseaseMolecular GeneticsDisease Gene IdentificationMedicine

References

	Year	Citations

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