hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome (Q37089623)
Jump to navigation
Jump to search
scientific article published on 20 September 2008
Language | Label | Description | Also known as |
---|---|---|---|
English | hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome |
scientific article published on 20 September 2008 |
Statements
hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome (English)
Akio Masuda
Xin-Ming Shen
Mikako Ito
Tohru Matsuura
Andrew G Engel
20 September 2008
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference