000 01363 a2200385 4500
005 20250516043207.0
264 0 _c20110830
008 201108s 0 0 eng d
022 _a1538-3652
024 7 _a10.1001/archdermatol.2011.138
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGruber, Robert
245 0 0 _aA novel homozygous missense mutation in SLURP1 causing Mal de Meleda with an atypical phenotype.
_h[electronic resource]
260 _bArchives of dermatology
_cJun 2011
300 _a748-50 p.
_bdigital
500 _aPublication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't
650 0 4 _aAcitretin
_xtherapeutic use
650 0 4 _aAdult
650 0 4 _aAnti-Infective Agents
_xtherapeutic use
650 0 4 _aAntigens, Ly
_xgenetics
650 0 4 _aBiopsy
650 0 4 _aHomozygote
650 0 4 _aHumans
650 0 4 _aKeratoderma, Palmoplantar
_xdiagnosis
650 0 4 _aKeratolytic Agents
_xtherapeutic use
650 0 4 _aMale
650 0 4 _aMutation, Missense
650 0 4 _aPhenotype
650 0 4 _aUrokinase-Type Plasminogen Activator
_xgenetics
700 1 _aHennies, Hans C
700 1 _aRomani, Nikolaus
700 1 _aSchmuth, Matthias
773 0 _tArchives of dermatology
_gvol. 147
_gno. 6
_gp. 748-50
856 4 0 _uhttps://doi.org/10.1001/archdermatol.2011.138
_zAvailable from publisher's website
999 _c20944845
_d20944845