Myasthenic syndromes in Turkish kinships due to mutations in the acetylcholine receptor
✍ Scribed by Kinji Ohno; Banu Anlar; Emire Özdirim; Joan M. Brengman; Jan L. DeBleecker; Dr. Andrew G. Engel
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 959 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0364-5134
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Congenital myasthenic syndrome comprises a heterogeneous group of inherited disorders of neuromuscular transmission. Acetylcholine receptor (AChR) deficiency is the most common form of congenital myasthenic syndrome and in most cases results from mutations within the coding region of the AChR subuni
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