000 01372 a2200385 4500
005 20250516001644.0
264 0 _c20101116
008 201011s 0 0 eng d
022 _a1552-4833
024 7 _a10.1002/ajmg.a.33648
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMorice-Picard, Fanny
245 0 0 _aA novel mutation in the fatty acid transport protein 4 gene in a patient initially described as affected by self-healing congenital verruciform hyperkeratosis.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cOct 2010
300 _a2664-5 p.
_bdigital
500 _aPublication Type: Letter
650 0 4 _aChild
650 0 4 _aFatty Acid Transport Proteins
_xgenetics
650 0 4 _aHumans
650 0 4 _aHyperkeratosis, Epidermolytic
_xgenetics
650 0 4 _aInfant, Newborn
650 0 4 _aInfant, Premature
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aMutation, Missense
650 0 4 _aRemission, Spontaneous
700 1 _aLéauté-Labrèze, Christine
700 1 _aDécor, Aude
700 1 _aBoralevi, Franck
700 1 _aLacombe, Didier
700 1 _aTaieb, Alain
700 1 _aFischer, Judith
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 152A
_gno. 10
_gp. 2664-5
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.33648
_zAvailable from publisher's website
999 _c20147968
_d20147968