Vesicular acetylcholine transporter defect underlies devastating congenital myasthenia syndrome. [electronic resource]
Producer: 20170522Description: 1021-1028 p. digitalISSN:- 1526-632X
- Adult
- Animals
- Arginine -- genetics
- Family Health
- Glycine -- genetics
- Humans
- Male
- Mice
- Mice, Transgenic
- Mutation -- genetics
- Myasthenic Syndromes, Congenital -- complications
- PC12 Cells
- Protein Processing, Post-Translational -- genetics
- RNA, Messenger
- Rats
- Transfection
- Vesicular Acetylcholine Transport Proteins -- genetics
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Publication Type: Case Reports; Journal Article
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