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A presynaptic congenital myasthenic syndrome attributed to a homozygous sequence variant in LAMA5.
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A presynaptic congenital myasthenic syndrome attributed to a homozygous sequence variant in LAMA5.
A presynaptic congenital myasthenic syndrome attributed to a homozygous sequence variant in LAMA5. Ann N Y Acad Sci. 2018 02; 1413(1):119-125.
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PubMed
subject areas
Adult
Female
Humans
Lambert-Eaton Myasthenic Syndrome
Laminin
Motor Endplate
Myasthenic Syndromes, Congenital
Synaptic Transmission
authors with profiles
Peter Pytel