000 01415 a2200373 4500
005 20250518084840.0
264 0 _c20210816
008 202108s 0 0 eng d
022 _a1563-5279
024 7 _a10.1080/00207454.2020.1730831
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aXu, Hongliang
245 0 0 _aSkin damage in a patient with lipid storage myopathy with a novel ETFDH mutation responsive to riboflavin.
_h[electronic resource]
260 _bThe International journal of neuroscience
_cDec 2020
300 _a1192-1198 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aElectron-Transferring Flavoproteins
_xgenetics
650 0 4 _aHumans
650 0 4 _aLipid Metabolism, Inborn Errors
_xdiagnosis
650 0 4 _aMultiple Acyl Coenzyme A Dehydrogenase Deficiency
_xdiagnosis
650 0 4 _aMuscular Dystrophies
_xdiagnosis
650 0 4 _aMutation, Missense
650 0 4 _aRiboflavin
_xadministration & dosage
650 0 4 _aSkin
_xpathology
650 0 4 _aVitamin B Complex
_xadministration & dosage
700 1 _aChen, Xin
700 1 _aLian, Yajun
700 1 _aWang, Shuya
700 1 _aJi, Tuo
700 1 _aZhang, Lu
700 1 _aLi, Shuang
773 0 _tThe International journal of neuroscience
_gvol. 130
_gno. 12
_gp. 1192-1198
856 4 0 _uhttps://doi.org/10.1080/00207454.2020.1730831
_zAvailable from publisher's website
999 _c30641367
_d30641367