SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably

Overview of attention for article published in Orphanet Journal of Rare Diseases, August 2022

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SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably https://t.co/4B08EP9qJT

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