Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood

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

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

When was Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood published?

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

What is the open-access status of Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood?

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

What is the DOI of Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood?

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.

What is the OpenAlex record for Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood?

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