000 01362 a2200385 4500
005 20250516050343.0
264 0 _c20120214
008 201202s 0 0 eng d
022 _a1365-2230
024 7 _a10.1111/j.1365-2230.2011.04138.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aIwamoto, K
245 0 0 _aA large heterozygous deletion including the entire C1 inhibitor gene in a sporadic case of hereditary angio-oedema.
_h[electronic resource]
260 _bClinical and experimental dermatology
_cJan 2012
300 _a20-3 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdult
650 0 4 _aAngioedemas, Hereditary
_xblood
650 0 4 _aAsian People
650 0 4 _aComplement C1 Inhibitor Protein
_xgenetics
650 0 4 _aExons
_xgenetics
650 0 4 _aFemale
650 0 4 _aFibrin Fibrinogen Degradation Products
_xanalysis
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aHumans
650 0 4 _aReal-Time Polymerase Chain Reaction
650 0 4 _aSequence Deletion
700 1 _aTanaka, A
700 1 _aKawai, M
700 1 _aIshii, K
700 1 _aMihara, S
700 1 _aHide, M
773 0 _tClinical and experimental dermatology
_gvol. 37
_gno. 1
_gp. 20-3
856 4 0 _uhttps://doi.org/10.1111/j.1365-2230.2011.04138.x
_zAvailable from publisher's website
999 _c21037078
_d21037078