Molecular basis of hereditary C1q deficiency—revisited: identification of several novel disease-causing mutations - Concepedia

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Molecular basis of hereditary C1q deficiency—revisited: identification of several novel disease-causing mutations

DOI Full Paper Access

104

Citations

27

References

2011

Year

Lone Schejbel, Lillemor Skattum, Stefan Hagelberg, Anders Åhlin, Bodil Schiller, Stefan Berg, Ferah Genel, Lennart Truedsson, Peter Garred

Genes and Immunity

Mendelian DisorderGenetic DisorderMedicineImmunodeficienciesGeneticsHereditary C1qPathologyMolecular GeneticsMolecular BasisDisease Gene IdentificationMolecular Diagnostics

References

	Year	Citations

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