Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood

Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood is a paper indexed in ScholarIQ from OpenAlex.

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Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood has 221 citations in the OpenAlex counts ScholarIQ stores.

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Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood has 2008 year in the ScholarIQ index.

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Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood has bronze oa status in the ScholarIQ index.

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The DOI for Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood is on the source record.

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The PMID for Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood is on the source record.

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The OpenAlex for Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood is on the source record.