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