PubMed:7191069 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/7191069","sourcedb":"PubMed","sourceid":"7191069","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/7191069","text":"Heterozygous C2-deficiency and myasthenia gravis.\nComplement 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 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