Characterizing a rare neurogenetic disease, SLC13A5 citrate transporter disorder, utilizing clinical data in a cloud-based medical record collection system
Spelbrink, Emily M, Brown, Tanya L, Brimble, Elise, Blanco, Kirsten A, Nye, Kimberly L, Porter, Brenda E
Published in Frontiers in genetics (21.03.2023)
Published in Frontiers in genetics (21.03.2023)
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