Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
November 1, 1996Human Molecular Genetics

An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene

View Full Paper
Ask AI
Bookmark
Share

Authors

DPD. Williams ParsonsBaylor College of Medicine

Discussion

Loading...

Member takes

Implication

Key Points

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

Cite This Study

D. Williams Parsons (1996) studied this question.

synapsesocial.com/papers/6a95a7dec473aeb83e676f47https://doi.org/10.1093/hmg/5.11.1727
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy1996 · 109 citations
  2. 2A simple salting out procedure for extracting DNA from human nucleated cells1988 · 20,617 citations
  3. 3Two 5q13 simple tandem repeat loci are in linkage disequilibrium with Type 1 spinal muscular atrophy1994 · 33 citations