Journal article

A novel syndrome of episodic muscle weakness maps to Xp22.3

MM Ryan, P Taylor, JA Donald, G Morgan, G Danta, MF Buckley, KN North

American Journal of Human Genetics | UNIV CHICAGO PRESS | Published : 1999

DOI: 10.1086/302588

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Keywords

Critical Region
X Chromosome
Periodic Paralysis
Genetic Linkage
Disorders
Paralyses, Familial Periodic
Chronic Disease
Male
Myasthenic Syndromes, Congenital
Pedigree
Choreoathetosis
Science & Technology
Familial Infantile Myasthenia
Crossing Over, Genetic
Adolescent
Phenotype
Infant
Female
Aged
Syndrome
Molecular Sequence Data
Life Sciences & Biomedicine
Potassium Channel Gene
Child
Cerebellar-Ataxia
Polymorphism, Genetic
Age of Onset
Adult
Humans
Muscle Weakness
Linkage
Genetics & Heredity
Diseases
Middle Aged
Child, Preschool
Lod Score
Chromosome 19p
Muscle, Skeletal