Published on
March 7, 2023
- 14:55 GMT
The TUDOR domain of SMN is an H3K79me1 histone mark reader
Spinal muscular atrophy is the leading genetic cause of infant mortality and results from depleted levels of functional survival of motor neuron (SMN) protein by either deletion or mutation of the SMN1 gene. SMN is characterized by a central TUDOR domain, …
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