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Paper published by Dr Farshid Parvini:
Case report
A Homozygous Truncating Mutation in NALCN Causing IHPRF1: Detailed Clinical Manifestations and a Review of Literature
Karimi AH, Karimi MR, Farnia P, Parvini F, Foroutan M
The Application of Clinical Genetics 2020, 13:151-157
Published Date: 27 August 2020