Maria Barile to Mutation
This is a "connection" page, showing publications Maria Barile has written about Mutation.
Connection Strength
0.155
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Leone P, Nisco A, de Gennaro L, Tolomeo M, Lorefice E, Petrosillo G, Russo S, De Giovanni D, Catacchio CR, Lepri FR, Ventura M, Simonetti S, Tummolo A, Barile M. Identification and Characterization of a Novel Biallelic SLC12A2 Variant Associated With Kilquist Syndrome (OMIM #619080). Am J Med Genet A. 2025 Dec; 197(12):e64188.
Score: 0.130
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Console L, Tolomeo M, Cosco J, Massey K, Barile M, Indiveri C. Impact of natural mutations on the riboflavin transporter 2 and their relevance to human riboflavin transporter deficiency 2. IUBMB Life. 2022 07; 74(7):618-628.
Score: 0.025