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Drosophila studies support a role for a presynaptic synaptotagmin mutation in a human congenital myasthenic syndrome

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Drosophila studies support a role for a presynaptic synaptotagmin mutation in a human congenital myasthenic syndrome is a paper indexed in PICO Portal from OpenAlex.

How many citations does Drosophila studies support a role for a presynaptic synaptotagmin mutation in a human congenital myasthenic syndrome have?

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Drosophila studies support a role for a presynaptic synaptotagmin mutation in a human congenital myasthenic syndrome has 14 citations in the OpenAlex counts PICO Portal stores.

When was Drosophila studies support a role for a presynaptic synaptotagmin mutation in a human congenital myasthenic syndrome published?

PICO Portalyear

Drosophila studies support a role for a presynaptic synaptotagmin mutation in a human congenital myasthenic syndrome has 2017 year in the PICO Portal index.

What is the open-access status of Drosophila studies support a role for a presynaptic synaptotagmin mutation in a human congenital myasthenic syndrome?

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Drosophila studies support a role for a presynaptic synaptotagmin mutation in a human congenital myasthenic syndrome has gold oa status in the PICO Portal index.

What is the DOI of Drosophila studies support a role for a presynaptic synaptotagmin mutation in a human congenital myasthenic syndrome?

PICO Portaldoi

The DOI for Drosophila studies support a role for a presynaptic synaptotagmin mutation in a human congenital myasthenic syndrome is on the source record.

What is the PMID of Drosophila studies support a role for a presynaptic synaptotagmin mutation in a human congenital myasthenic syndrome?

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The PMID for Drosophila studies support a role for a presynaptic synaptotagmin mutation in a human congenital myasthenic syndrome is on the source record.

What is the OpenAlex record for Drosophila studies support a role for a presynaptic synaptotagmin mutation in a human congenital myasthenic syndrome?

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The OpenAlex for Drosophila studies support a role for a presynaptic synaptotagmin mutation in a human congenital myasthenic syndrome is on the source record.

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