Genetic screen identifies a requirement for SMN in mRNA localisation within the Drosophila oocyte
Abstract Objective Spinal muscular atrophy (SMA) results from insufficient levels of the survival motor neuron (SMN) protein. Drosophila is conducive to large-scale genetic-modifier screens which can reveal novel pathways underpinning the disease mechanism. We tested the ability of a large collectio...
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
BMC
2018-06-01
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Series: | BMC Research Notes |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s13104-018-3496-1 |