Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
November 1, 1998Human Molecular Genetics

The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophy

View Full Paper
Ask AI
Bookmark
Share

Authors

PBP BurletHôpital Necker-Enfants MaladesCHCéline HuberHôpital Necker-Enfants MaladesSBSolange BertrandyInstitut Jacques Monod

Discussion

Loading...

Member takes

Implication

Key Points

Key points are not available for this paper at this time.

Cite This Study

Burlet et al. (1998) studied this question.

synapsesocial.com/papers/69dd61dc7808b00a4799d6c6https://doi.org/10.1093/hmg/7.12.1927
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1The survival motor neuron protein in spinal muscular atrophy1997 · 724 citations
  2. 2Frameshift mutation in the survival motor neuron gene in a severe case of SMA type I1996 · 92 citations
  3. 3Missense mutation clustering in the survival motor neuron gene: a role for a conserved tyrosine and glycine rich region of the protein in RNA metabolism?1997 · 156 citations
  4. 4The Spinal Muscular Atrophy Disease Gene Product, SMN, and Its Associated Protein SIP1 Are in a Complex with Spliceosomal snRNP Proteins1997 · 661 citations
  5. 5Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy1995 · 229 citations