000 01478 a2200397 4500
005 20250517175656.0
264 0 _c20180305
008 201803s 0 0 eng d
022 _a1460-2083
024 7 _a10.1093/hmg/ddx215
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aWood, Matthew J A
245 0 0 _aSpinal muscular atrophy: antisense oligonucleotide therapy opens the door to an integrated therapeutic landscape.
_h[electronic resource]
260 _bHuman molecular genetics
_c10 2017
300 _aR151-R159 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aAnimals
650 0 4 _aCentral Nervous System
_xmetabolism
650 0 4 _aDisease Models, Animal
650 0 4 _aExons
650 0 4 _aHumans
650 0 4 _aMice
650 0 4 _aMotor Neurons
_xmetabolism
650 0 4 _aMuscular Atrophy, Spinal
_xgenetics
650 0 4 _aOligodeoxyribonucleotides, Antisense
_xgenetics
650 0 4 _aOligonucleotides
_xtherapeutic use
650 0 4 _aOligonucleotides, Antisense
_xadministration & dosage
650 0 4 _aRNA, Messenger
_xgenetics
650 0 4 _aSpinal Cord
_xmetabolism
650 0 4 _aSurvival of Motor Neuron 1 Protein
_xgenetics
650 0 4 _aSurvival of Motor Neuron 2 Protein
_xgenetics
700 1 _aTalbot, Kevin
700 1 _aBowerman, Melissa
773 0 _tHuman molecular genetics
_gvol. 26
_gno. R2
_gp. R151-R159
856 4 0 _uhttps://doi.org/10.1093/hmg/ddx215
_zAvailable from publisher's website
999 _c27630970
_d27630970