000 01409 a2200421 4500
005 20250518050500.0
264 0 _c20200427
008 202004s 0 0 eng d
022 _a1750-1172
024 7 _a10.1186/s13023-019-1140-3
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLópez-Sainz, Ángela
245 0 0 _aNegative screening of Fabry disease in patients with conduction disorders requiring a pacemaker.
_h[electronic resource]
260 _bOrphanet journal of rare diseases
_c07 2019
300 _a170 p.
_bdigital
500 _aPublication Type: Letter; Research Support, Non-U.S. Gov't
650 0 4 _aAged
650 0 4 _aCardiomyopathy, Hypertrophic
_xgenetics
650 0 4 _aEchocardiography
650 0 4 _aFabry Disease
_xdiagnosis
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMutation
_xgenetics
650 0 4 _aPacemaker, Artificial
700 1 _aCliment, Vicente
700 1 _aRipoll-Vera, Tomas
700 1 _aEspinosa, Maria Angeles
700 1 _aBarriales-Villa, Roberto
700 1 _aNavarro, Marina
700 1 _aLimeres, Javier
700 1 _aDomingo, Diana
700 1 _aKasper, David C
700 1 _aGarcia-Pavia, Pablo
773 0 _tOrphanet journal of rare diseases
_gvol. 14
_gno. 1
_gp. 170
856 4 0 _uhttps://doi.org/10.1186/s13023-019-1140-3
_zAvailable from publisher's website
999 _c29882904
_d29882904