Clinical characteristics of a group of Turkish patients having a benign CMS phenotype with ptosis and marked ophthalmoparesis and mutations in the acetylcholine receptor epsilon subunit gene

Acta Myologica

Volumn 19, Issue APR., 2000, Pages 29-32

  Deymeer, F ^a   Serdaroglu, P ^a   Gulsen Parman, Y ^a   Ozturk, A ^a   Ozdemir, C ^a  

^a ISTANBUL UNIVERSITY   (Turkey)

Author keywords

Congenital myasthenic syndromes; Epsilon subunit mutations; Ophthalmoparesis

Indexed keywords

CHOLINERGIC RECEPTOR;

ARTICLE; CLINICAL ARTICLE; DIFFERENTIAL DIAGNOSIS; EATON LAMBERT SYNDROME; FEMALE; GENE MUTATION; HUMAN; MALE; MYASTHENIA GRAVIS; OPHTHALMOPLEGIA; PHENOTYPE; TURKEY (REPUBLIC);

EID: 0033948598     PISSN: 11282460     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (18)