Mutations causing congenital myasthenia reveal principal coupling pathway in the acetylcholine receptor ε-subunit. [electronic resource]
Producer: 20191028ISSN:- 2379-3708
- Adult
- Arginine -- genetics
- Consanguinity
- DNA Mutational Analysis
- Evoked Potentials, Motor -- physiology
- Female
- Glutamic Acid -- genetics
- HEK293 Cells
- Homozygote
- Humans
- Muscle, Skeletal -- pathology
- Mutation
- Myasthenic Syndromes, Congenital -- genetics
- Patch-Clamp Techniques
- Receptors, Nicotinic -- genetics
- Recombinant Proteins -- genetics
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural
There are no comments on this title.
Log in to your account to post a comment.