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DRDQ haplotypes determine clinical forms of myasthenia gravis

✍ Scribed by Pirskanen, Ritva; Carlsson, Björn; Lefvert, Ann-Kari; Matell, Georg; Olerup, Olle; Smith, Edvard

Book ID: 122539211
Publisher: Elsevier Science
Year: 1991
Tongue: English
Weight: 87 KB
Volume: 4
Category: Article
ISSN: 0896-8411
DOI: 10.1016/0896-8411(91)90089-U

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## Abstract Myasthenia gravis (MG) is a syndrome of fluctuating skeletal muscle weakness that worsens with use and improves with rest. Eye, facial, oropharyngeal, axial, and limb muscles may be involved in varying combinations and degrees of severity. Its etiology is heterogeneous, divided initiall