Congenital Myasthenic Syndrome (CMS) Type Ia: Clinical and Genetic Diversity

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Bibliographic Details
Published in:Annals of the New York Academy of Sciences 1998-05, Vol.841 (1), p.157-166
Main Authors: MIDDLETON, LEFKOS T., CHRISTODOULOU, KYPROULA, DEYMEER, FESA, SERDAROGLU, PIRAYE, OZDEMIR, COSKUN, AL-QUDAH, ABDEL KARIM, AL-SHEHAB, AHMAD, MAVROMATIS, IOANNIS, MYLONAS, IOANNIS, EVOLI, AMELIA, TSINGIS, MARIOS, ZAMBA, ELENI, KYRIALLIS, KYRIAKOS
Format: Article
Language:English
Subjects:
Adolescent
Adult
Child
Child, Preschool
Chromosome Mapping
Chromosomes, Human, Pair 17
Electrodiagnosis
Female
Genes, Dominant
Genes, Recessive
Genetic Linkage
Genetic Variation
Humans
Lod Score
Male
Microsatellite Repeats
Middle Aged
Myasthenia Gravis - congenital
Myasthenia Gravis - genetics
Myasthenia Gravis - physiopathology
Pedigree
Receptors, Cholinergic - deficiency
Receptors, Cholinergic - genetics
Syndrome
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ISSN:0077-8923
1749-6632
DOI:10.1111/j.1749-6632.1998.tb10922.x