2010
DOI: 10.1016/s0960-8966(10)70034-1
|View full text |Cite
|
Sign up to set email alerts
|

P19 An extremely high rate of de novo base substitution mutations causes interruptions at the myotonic dystrophy type 1 locus

Help me understand this report

This publication either has no citations yet, or we are still processing them

Set email alert for when this publication receives citations?

See others like this or search for similar articles