Repository of Research and Investigative Information

Repository of Research and Investigative Information

Zabol University of Medical Sciences

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Items where Author is "Abrams, C. K."

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(2022) Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders. Orphanet Journal of Rare Diseases. p. 18.

(2022) Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders. Orphanet Journal of Rare Diseases. ISSN 17501172 (ISSN)

This list was generated on Fri May 3 19:36:34 2024 IRDT.
Repository of Research and Investigative InformationZabol University of Medical Sciences

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