000 01446 a2200445 4500
005 20250517091305.0
264 0 _c20170217
008 201702s 0 0 eng d
022 _a1873-3492
024 7 _a10.1016/j.cca.2016.04.004
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLv, Fang
245 0 0 _aA novel mutation in CLDN16 results in rare familial hypomagnesaemia with hypercalciuria and nephrocalcinosis in a Chinese family.
_h[electronic resource]
260 _bClinica chimica acta; international journal of clinical chemistry
_cJun 2016
300 _a69-74 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdolescent
650 0 4 _aChild
650 0 4 _aChina
650 0 4 _aClaudins
_xgenetics
650 0 4 _aEthnicity
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aHypercalciuria
_xcomplications
650 0 4 _aMagnesium
_xblood
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aNephrocalcinosis
_xcomplications
650 0 4 _aPedigree
700 1 _aXu, Xiao-Jie
700 1 _aWang, Jian-Yi
700 1 _aLiu, Yi
700 1 _aJiang, Yan
700 1 _aWang, Ou
700 1 _aXia, Wei-Bo
700 1 _aXing, Xiao-Ping
700 1 _aLi, Mei
773 0 _tClinica chimica acta; international journal of clinical chemistry
_gvol. 457
_gp. 69-74
856 4 0 _uhttps://doi.org/10.1016/j.cca.2016.04.004
_zAvailable from publisher's website
999 _c25915028
_d25915028