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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Heterozygous C2-deficiency and myasthenia gravis.

Complement deficiency states in myasthenia gravis (MG) have not been reported previously. We describe a 19-year-old woman with typical MG and heterozygous C2 deficiency, along with HLA typing of the patient and her immediate family.[1]


  1. Heterozygous C2-deficiency and myasthenia gravis. Riggs, J.E., Griggs, R.C., Rosenfeld, S.I., May, A.G., Penn, A.S. Neurology (1980) [Pubmed]
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