Repository of Research and Investigative Information

Repository of Research and Investigative Information

Hamadan University of Medical Sciences

Items where Author is "Antony, D."

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Article

(2018) Parental Whole-Exome Sequencing Enables Sialidosis Type II Diagnosis due to an NEU1 Missense Mutation as an Underlying Cause of Nephrotic Syndrome in the Child. Kidney International Reports. ISSN 24680249

This list was generated on Sun Jul 5 21:43:30 2020 IRDT.