000 | 01192 a2200325 4500 | ||
---|---|---|---|
005 | 20250516120218.0 | ||
264 | 0 | _c20130410 | |
008 | 201304s 0 0 eng d | ||
022 | _a1750-1172 | ||
024 | 7 |
_a10.1186/1750-1172-7-83 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aBosch, Annet M | |
245 | 0 | 0 |
_aThe Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives. _h[electronic resource] |
260 |
_bOrphanet journal of rare diseases _cOct 2012 |
||
300 |
_a83 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Review | ||
650 | 0 | 4 |
_aBulbar Palsy, Progressive _xdrug therapy |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 |
_aHearing Loss, Sensorineural _xdrug therapy |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMale |
650 | 0 | 4 |
_aRiboflavin _xtherapeutic use |
700 | 1 | _aStroek, Kevin | |
700 | 1 | _aAbeling, Nico G | |
700 | 1 | _aWaterham, Hans R | |
700 | 1 | _aIjlst, Lodewijk | |
700 | 1 | _aWanders, Ronald J A | |
773 | 0 |
_tOrphanet journal of rare diseases _gvol. 7 _gp. 83 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1186/1750-1172-7-83 _zAvailable from publisher's website |
999 |
_c22221396 _d22221396 |