000 01246 a2200361 4500
005 20250515091028.0
264 0 _c20080410
008 200804s 0 0 eng d
022 _a0007-0963
024 7 _a10.1111/j.1365-2133.2007.08219.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMartignago, B C F
245 0 0 _aRecurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome.
_h[electronic resource]
260 _bThe British journal of dermatology
_cDec 2007
300 _a1281-4 p.
_bdigital
500 _aPublication Type: Letter; Research Support, Non-U.S. Gov't
650 0 4 _aFemale
650 0 4 _aGenetic Carrier Screening
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMembrane Proteins
_xgenetics
650 0 4 _aMutation
_xgenetics
650 0 4 _aNeoplasm Proteins
_xgenetics
650 0 4 _aPedigree
650 0 4 _aSkin Diseases, Genetic
_xgenetics
650 0 4 _aSyndrome
700 1 _aLai-Cheong, J E
700 1 _aLiu, L
700 1 _aMcGrath, J A
700 1 _aCestari, T F
773 0 _tThe British journal of dermatology
_gvol. 157
_gno. 6
_gp. 1281-4
856 4 0 _uhttps://doi.org/10.1111/j.1365-2133.2007.08219.x
_zAvailable from publisher's website
999 _c17437701
_d17437701