Molecular and phenotypic reassessment of an infrequently used mouse model for spinal muscular atrophy
Główni autorzy: | Gogliotti, R, Hammond, S, Lutz, C, DiDonato, C |
---|---|
Format: | Journal article |
Wydane: |
2010
|
Podobne zapisy
-
A Short Antisense Oligonucleotide Ameliorates Symptoms of Severe Mouse Models of Spinal Muscular Atrophy
od: Jeffrey M Keil, i wsp.
Wydane: (2014-01-01) -
In Search of a Cure: The Development of Therapeutics to Alter the Progression of Spinal Muscular Atrophy
od: Kristine S. Ojala, i wsp.
Wydane: (2021-02-01) -
Spinal muscular atrophy-like phenotype in a mouse model of acid ceramidase deficiency
od: Murtaza S. Nagree, i wsp.
Wydane: (2023-05-01) -
Abnormal motor phenotype in the SMNΔ7 mouse model of spinal muscular atrophy
od: Matthew E.R. Butchbach, i wsp.
Wydane: (2007-08-01) -
Clinical Phenotyping and Biomarkers in Spinal and Bulbar Muscular Atrophy
od: Elina Millere, i wsp.
Wydane: (2021-01-01)