Congenital myasthenic syndrome. (CMS) type Ia. Clinical and genetic diversity. [electronic resource]
Producer: 19980804Description: 157-66 p. digitalISSN:- 0077-8923
- 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
- Pedigree
- Receptors, Cholinergic -- deficiency
- Syndrome
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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