Novel causative variants in Legius syndrome: SPRED1 Genotype spectrum expansion.
Chelleri C, Brolatti N, De Marco P, Ognibene M, Diana MC, Madia F, Duca MD, Santangelo A, Capra V, Striano P, Zara F, Scala M.
Chelleri C, et al. Among authors: duca md.
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Am J Med Genet A. 2024.
PMID: 39031930