Commonality amid diversity: Multi-study proteomic identification of conserved disease mechanisms in spinal muscular atrophy
Author:
Funder
SMA Trust
BBSRC
MRC
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference68 articles.
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4. Identification and characterization of a spinal muscular atrophy-determining gene;Lefebvre;Cell,1995
5. SMN oligomerization defect correlates with spinal muscular atrophy severity;Lorson;Nat Genet,1998
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