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Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology

PaperCitations, authors & open-access status

Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology is a paper indexed in PICO Portal from OpenAlex.

How many citations does Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology have?

PICO Portalcitation count

Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology has 231 citations in the OpenAlex counts PICO Portal stores.

When was Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology published?

PICO Portalyear

Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology has 2013 year in the PICO Portal index.

What is the open-access status of Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology?

PICO Portaloa status

Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology has green oa status in the PICO Portal index.

What is the DOI of Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology?

PICO Portaldoi

The DOI for Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology is on the source record.

What is the PMID of Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology?

PICO Portalpmid

The PMID for Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology is on the source record.

What is the OpenAlex record for Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology?

PICO Portalopenalex

The OpenAlex for Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology is on the source record.

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