000 01581 a2200469 4500
005 20250514184809.0
264 0 _c20041019
008 200410s 0 0 eng d
022 _a1552-4825
024 7 _a10.1002/ajmg.a.20660
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBarth, Peter G
245 0 0 _aX-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cMay 2004
300 _a349-54 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aAcyltransferases
650 0 4 _aCardiolipins
_xanalysis
650 0 4 _aCardiomyopathy, Dilated
_xpathology
650 0 4 _aFemale
650 0 4 _aGenetic Diseases, X-Linked
_xgenetics
650 0 4 _aHumans
650 0 4 _aLipids
_xblood
650 0 4 _aMale
650 0 4 _aMuscular Diseases
_xpathology
650 0 4 _aMutation
650 0 4 _aNeutropenia
_xpathology
650 0 4 _aPedigree
650 0 4 _aProteins
_xgenetics
650 0 4 _aSurvival Rate
650 0 4 _aSyndrome
650 0 4 _aTranscription Factors
_xgenetics
700 1 _aValianpour, Fredoen
700 1 _aBowen, Valerie M
700 1 _aLam, Jan
700 1 _aDuran, Marinus
700 1 _aVaz, Frédéric M
700 1 _aWanders, Ronald J A
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 126A
_gno. 4
_gp. 349-54
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.20660
_zAvailable from publisher's website
999 _c14810002
_d14810002