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Characterisation of nucleotide sequence variants and disease-specific mutations involving the 3' end of the C1-inhibitor gene in hereditary angio-oedema.
Siddique, Z; McPhaden, A R; Whaley, K.
Affiliation
  • Siddique Z; University Department of Pathology, Western Infirmary, Glasgow, UK.
Hum Hered ; 45(2): 98-102, 1995.
Article in En | MEDLINE | ID: mdl-7750982
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Complement C1 Inactivator Proteins / Angioedema / Mutation Type of study: Prognostic_studies Limits: Humans Language: En Journal: Hum Hered Year: 1995 Document type: Article Affiliation country: Reino Unido Country of publication: Suiza
Search on Google
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Complement C1 Inactivator Proteins / Angioedema / Mutation Type of study: Prognostic_studies Limits: Humans Language: En Journal: Hum Hered Year: 1995 Document type: Article Affiliation country: Reino Unido Country of publication: Suiza