000 01542 a2200469 4500
005 20250517140405.0
264 0 _c20180110
008 201801s 0 0 eng d
022 _a1873-3492
024 7 _a10.1016/j.cca.2017.02.007
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLv, Fang
245 0 0 _aRecurrent and novel mutations in the NTRK1 gene lead to rare congenital insensitivity to pain with anhidrosis in two Chinese patients.
_h[electronic resource]
260 _bClinica chimica acta; international journal of clinical chemistry
_cMay 2017
300 _a39-45 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAmino Acid Sequence
650 0 4 _aAnimals
650 0 4 _aAsian People
_xgenetics
650 0 4 _aBase Sequence
650 0 4 _aChild
650 0 4 _aFemale
650 0 4 _aHereditary Sensory and Autonomic Neuropathies
_xenzymology
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aPedigree
650 0 4 _aPhenotype
650 0 4 _aReceptor, trkA
_xchemistry
650 0 4 _aYoung Adult
700 1 _aXu, Xiao-Jie
700 1 _aSong, Yu-Wen
700 1 _aLi, Lu-Jiao
700 1 _aWang, Ou
700 1 _aJiang, Yan
700 1 _aXia, Wei-Bo
700 1 _aXing, Xiao-Ping
700 1 _aGao, Peng
700 1 _aLi, Mei
773 0 _tClinica chimica acta; international journal of clinical chemistry
_gvol. 468
_gp. 39-45
856 4 0 _uhttps://doi.org/10.1016/j.cca.2017.02.007
_zAvailable from publisher's website
999 _c26875032
_d26875032