000 01123 a2200301 4500
005 20250518093114.0
264 0 _c20210514
008 202105s 0 0 eng d
022 _a1468-3083
024 7 _a10.1111/jdv.16384
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aChihara, M
245 0 0 _aA novel mutation in the KCNJ8 gene encoding the Kir6.1 subunit of an ATP-sensitive potassium channel in a Japanese patient with CantĂș syndrome.
_h[electronic resource]
260 _bJournal of the European Academy of Dermatology and Venereology : JEADV
_cSep 2020
300 _ae476-e478 p.
_bdigital
500 _aPublication Type: Letter
650 0 4 _aCardiomegaly
650 0 4 _aHumans
650 0 4 _aHypertrichosis
_xgenetics
650 0 4 _aJapan
650 0 4 _aKATP Channels
_xgenetics
650 0 4 _aMutation
650 0 4 _aOsteochondrodysplasias
700 1 _aAsahina, A
700 1 _aItoh, M
773 0 _tJournal of the European Academy of Dermatology and Venereology : JEADV
_gvol. 34
_gno. 9
_gp. e476-e478
856 4 0 _uhttps://doi.org/10.1111/jdv.16384
_zAvailable from publisher's website
999 _c30783991
_d30783991