PubMed:7191069 / 0-49 JSON TXT

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.

projects that have annotations to this span

Unselected / annnotation		Selected / annnotation
sentences 2 (2) PubCasesORDO 1 (1) NCBIDiseaseCorpus 2 (2) NCBI-Disease-Train 2 (2) NCBI-Disease-Corpus-All 2 (2) NCBI-Disease-Corpus-2stage-All 1 (1) NCBI-Disease-Corpus-rezarta-All 2 (2) NCBI-Disease-Corpus-4oGuideline-All 2 (2) NCBI-Disease-Corpus-Simple-All 1 (1)

TAB JSON ListView MergeView

PubMed:7191069 / 0-49 JSONTXT

projects that have annotations to this span

PubMed:7191069 / 0-49 JSON TXT