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Erratum: Detection of C1 inhibitor (SERPING1/C1NH) mutations in exon 8 in patients with hereditary angioedema: evidence for 10 novel mutations
Author(s) -
Blanch Alvaro,
Roche Olga,
LópezGranados Eduardo,
Fontán Gumersindo,
LópezTrascasa Margarita
Publication year - 2003
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/humu.9105
Subject(s) - regret , biology , exon , mutation , genetics , gene , computer science , machine learning
The original article to which this Erratum refers was published in Human Mutation 20:405–406 Human Mutation (2002) 20(5) 405–406 The authors regret that there was an error in Table 2 on Page 4 of the original article. In patient DS, the nucleotide change 16838C>T is not correct. It should be 16838G>A, since this was the mutation at the antisense change.

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