000 01629 a2200481 4500
005 20250516152347.0
264 0 _c20140324
008 201403s 0 0 eng d
022 _a1439-3824
024 7 _a10.1055/s-0033-1343482
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHainmann, I
245 0 0 _aCoincidence of 2 severe chronic diseases: presymptomatic diagnosis of Wilson disease in a boy with severe haemophilia A.
_h[electronic resource]
260 _bKlinische Padiatrie
_cMay 2013
300 _a174-5 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdenosine Triphosphatases
_xgenetics
650 0 4 _aCation Transport Proteins
_xgenetics
650 0 4 _aChromosome Deletion
650 0 4 _aChromosome Inversion
650 0 4 _aCopper-Transporting ATPases
650 0 4 _aDNA Mutational Analysis
650 0 4 _aEarly Diagnosis
650 0 4 _aFactor VIII
_xgenetics
650 0 4 _aGenetic Carrier Screening
650 0 4 _aHemophilia A
_xcomplications
650 0 4 _aHepatolenticular Degeneration
_xcomplications
650 0 4 _aHumans
650 0 4 _aIntrons
650 0 4 _aLiver Function Tests
650 0 4 _aMale
650 0 4 _aPenicillamine
_xtherapeutic use
650 0 4 _aUltrasonography
650 0 4 _aVitamin B 6
_xtherapeutic use
700 1 _aWoltering, T
700 1 _aGreiner, P
700 1 _aNakamura, L
700 1 _aPodskarbi, T
700 1 _aOldenburg, J
700 1 _aZieger, B
773 0 _tKlinische Padiatrie
_gvol. 225
_gno. 3
_gp. 174-5
856 4 0 _uhttps://doi.org/10.1055/s-0033-1343482
_zAvailable from publisher's website
999 _c22782123
_d22782123