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The Lancet. Neurology
|
August 29, 2009
Local restoration of dystrophin expression with the morpholino oligomer AVI-4658 in Duchenne muscular dystrophy: a single-blind, placebo-controlled, dose-escalation, proof-of-concept study
Maria Kinali, Virginia Arechavala-Gomeza, Lucy Feng, et al.
Life Science Alliance
|
August 14, 2021
Dystrophin involvement in peripheral circadian SRF signalling
Corinne A Betts, Aarti Jagannath, Tirsa LE van Westering, et al.
Brain : a Journal of Neurology
|
December 25, 2015
Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy
Irina T Zaharieva, Michael G Thor, Emily C Oates, et al.
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of 8
Search research articles
Search
Showing results (71-80 of 73) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 73 results.
The Lancet. Neurology
|
August 29, 2009
Local restoration of dystrophin expression with the morpholino oligomer AVI-4658 in Duchenne muscular dystrophy: a single-blind, placebo-controlled, dose-escalation, proof-of-concept study
Maria Kinali, Virginia Arechavala-Gomeza, Lucy Feng, et al.
Life Science Alliance
|
August 14, 2021
Dystrophin involvement in peripheral circadian SRF signalling
Corinne A Betts, Aarti Jagannath, Tirsa LE van Westering, et al.
Brain : a Journal of Neurology
|
December 25, 2015
Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy
Irina T Zaharieva, Michael G Thor, Emily C Oates, et al.
Page
of 8