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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

University of Melbourne Researchers

Kathryn North's Profile Picture
Kathryn North Author Paediatrics Royal Children's Hospital

Monique Ryan's Profile Picture
Monique Ryan Author Paediatrics Royal Children's Hospital

Citation metrics

6Web of Science
10Scopus

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

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