A natural history study of late onset spinal muscular atrophy types 3b and 4.

Subjects

Subjects :

DCN 2: Functional Neurogenomics.
IGMD 3: Genomic disorders and inherited multi-system disorders.
NCEBP 10: Human Movement & Fatigue.
UMCN 3.1: Neuromuscular development and genetic disorders.
UMCN 5.1: Genetic defects of metabolism.

Details

Database :

OAIster

Notes :

Berg, L.H. van den author., Brugman, F. author., Scheffer, H. author., Ruiterkamp-Versteeg, M. author., Engelen, B.G.M. van author., Faber, C.G. author., Visser, M. de author., Pol, W.L. van der author., Wokke, J.H.J. author.

Accession number :

edsoai.on1443213575