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Melanoma cases demonstrate increased carrier frequency of phenylketonuria/hyperphenylalanemia mutations

PaperCitations, authors & open-access status

Melanoma cases demonstrate increased carrier frequency of phenylketonuria/hyperphenylalanemia mutations is a paper indexed in PICO Portal from OpenAlex.

How many citations does Melanoma cases demonstrate increased carrier frequency of phenylketonuria/hyperphenylalanemia mutations have?

PICO Portalcitation count

Melanoma cases demonstrate increased carrier frequency of phenylketonuria/hyperphenylalanemia mutations has 11 citations in the OpenAlex counts PICO Portal stores.

When was Melanoma cases demonstrate increased carrier frequency of phenylketonuria/hyperphenylalanemia mutations published?

PICO Portalyear

Melanoma cases demonstrate increased carrier frequency of phenylketonuria/hyperphenylalanemia mutations has 2018 year in the PICO Portal index.

What is the open-access status of Melanoma cases demonstrate increased carrier frequency of phenylketonuria/hyperphenylalanemia mutations?

PICO Portaloa status

Melanoma cases demonstrate increased carrier frequency of phenylketonuria/hyperphenylalanemia mutations has green oa status in the PICO Portal index.

What is the DOI of Melanoma cases demonstrate increased carrier frequency of phenylketonuria/hyperphenylalanemia mutations?

PICO Portaldoi

The DOI for Melanoma cases demonstrate increased carrier frequency of phenylketonuria/hyperphenylalanemia mutations is on the source record.

What is the PMID of Melanoma cases demonstrate increased carrier frequency of phenylketonuria/hyperphenylalanemia mutations?

PICO Portalpmid

The PMID for Melanoma cases demonstrate increased carrier frequency of phenylketonuria/hyperphenylalanemia mutations is on the source record.

What is the OpenAlex record for Melanoma cases demonstrate increased carrier frequency of phenylketonuria/hyperphenylalanemia mutations?

PICO Portalopenalex

The OpenAlex for Melanoma cases demonstrate increased carrier frequency of phenylketonuria/hyperphenylalanemia mutations is on the source record.

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