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 |