000 01121 a2200325 4500
005 20250517010341.0
264 0 _c20160531
008 201605s 0 0 eng d
022 _a2240-2993
024 7 _a10.1007/s13760-014-0405-9
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aYiş, Uluç
245 0 0 _aA novel NTRK1 mutation in a patient with congenital insensitivity to pain with anhidrosis.
_h[electronic resource]
260 _bActa neurologica Belgica
_cSep 2015
300 _a509-11 p.
_bdigital
500 _aPublication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't
650 0 4 _aBase Sequence
650 0 4 _aChild
650 0 4 _aHereditary Sensory and Autonomic Neuropathies
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aPedigree
650 0 4 _aReceptor, trkA
_xgenetics
700 1 _aMademan, Inès
700 1 _aKavukçu, Salih
700 1 _aBaets, Jonathan
773 0 _tActa neurologica Belgica
_gvol. 115
_gno. 3
_gp. 509-11
856 4 0 _uhttps://doi.org/10.1007/s13760-014-0405-9
_zAvailable from publisher's website
999 _c24467978
_d24467978