000 | 01928 a2200601 4500 | ||
---|---|---|---|
005 | 20250516052229.0 | ||
264 | 0 | _c20120111 | |
008 | 201201s 0 0 eng d | ||
022 | _a1878-0849 | ||
024 | 7 |
_a10.1016/j.ejmg.2011.07.005 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aMillat, Gilles | |
245 | 0 | 0 |
_aClinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy. _h[electronic resource] |
260 |
_bEuropean journal of medical genetics _c |
||
300 |
_ae570-5 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aAdult |
650 | 0 | 4 |
_aArrhythmias, Cardiac _xetiology |
650 | 0 | 4 |
_aCardiomyopathy, Dilated _xcomplications |
650 | 0 | 4 | _aCohort Studies |
650 | 0 | 4 | _aDNA Mutational Analysis |
650 | 0 | 4 | _aEarly Diagnosis |
650 | 0 | 4 | _aExons |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aFrance |
650 | 0 | 4 | _aGenetic Testing |
650 | 0 | 4 | _aGenotype |
650 | 0 | 4 |
_aHeart Conduction System _xpathology |
650 | 0 | 4 | _aHeterozygote |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aLamin Type A _xgenetics |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMiddle Aged |
650 | 0 | 4 | _aMutation |
650 | 0 | 4 | _aPedigree |
650 | 0 | 4 | _aPhenotype |
650 | 0 | 4 |
_aSequence Analysis, DNA _xmethods |
700 | 1 | _aBouvagnet, Patrice | |
700 | 1 | _aChevalier, Philippe | |
700 | 1 | _aSebbag, Laurent | |
700 | 1 | _aDulac, Arnaud | |
700 | 1 | _aDauphin, Claire | |
700 | 1 | _aJouk, Pierre-Simon | |
700 | 1 | _aDelrue, Marie-Ange | |
700 | 1 | _aThambo, Jean-Benoit | |
700 | 1 | _aLe Metayer, Philippe | |
700 | 1 | _aSeronde, Marie-France | |
700 | 1 | _aFaivre, Laurence | |
700 | 1 | _aEicher, Jean-Christophe | |
700 | 1 | _aRousson, Robert | |
773 | 0 |
_tEuropean journal of medical genetics _gvol. 54 _gno. 6 _gp. e570-5 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.ejmg.2011.07.005 _zAvailable from publisher's website |
999 |
_c21090221 _d21090221 |