| 000 | 01783 a2200529 4500 | ||
|---|---|---|---|
| 005 | 20250518055712.0 | ||
| 264 | 0 | _c20210723 | |
| 008 | 202107s 0 0 eng d | ||
| 022 | _a1559-1174 | ||
| 024 | 7 |
_a10.1007/s12017-019-08564-4 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aDeng, Sheng | |
| 245 | 0 | 0 |
_aIncidence and Clinical Features of TRPV4-Linked Axonal Neuropathies in a USA Cohort of Charcot-Marie-Tooth Disease Type 2. _h[electronic resource] |
| 260 |
_bNeuromolecular medicine _c03 2020 |
||
| 300 |
_a68-72 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aAxons _xpathology |
| 650 | 0 | 4 |
_aBone Diseases, Developmental _xetiology |
| 650 | 0 | 4 |
_aCharcot-Marie-Tooth Disease _xepidemiology |
| 650 | 0 | 4 |
_aExons _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Counseling |
| 650 | 0 | 4 |
_aHearing Loss _xetiology |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIncidence |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMuscle Weakness _xetiology |
| 650 | 0 | 4 |
_aMuscular Atrophy, Spinal _xepidemiology |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPoint Mutation |
| 650 | 0 | 4 |
_aTRPV Cation Channels _xdeficiency |
| 650 | 0 | 4 |
_aUnited States _xepidemiology |
| 650 | 0 | 4 |
_aVocal Cord Paralysis _xetiology |
| 700 | 1 | _aFeely, Shawna M E | |
| 700 | 1 | _aShi, Yong | |
| 700 | 1 | _aZhai, Hong | |
| 700 | 1 | _aZhan, Luna | |
| 700 | 1 | _aSiddique, Teepu | |
| 700 | 1 | _aDeng, Han-Xiang | |
| 700 | 1 | _aShy, Michael E | |
| 773 | 0 |
_tNeuromolecular medicine _gvol. 22 _gno. 1 _gp. 68-72 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s12017-019-08564-4 _zAvailable from publisher's website |
| 999 |
_c30060230 _d30060230 |
||