A novel missense mutation in GREB1L identified in a three-generation family with renal hypodysplasia/aplasia-3

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

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A novel missense mutation in GREB1L identified in a three-generation family with renal hypodysplasia/aplasia-3 https://t.co/voufwTMYEA

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