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Journal: Genes, 2022
Volume: 13
Number: 252
252
Article: SPECC1L Mutations Are Not Common in Sporadic Cases of Opitz G/BBB Syndrome
Authors: by Chiara Migliore, Anna Vendramin, Shane McKee, Paolo Prontera, Francesca Faravelli, Rani Sachdev, Patricia Dias, Martina Mascaro, Danilo Licastro and Germana Meroni
Link: https://www.mdpi.com/2073-4425/13/2/252

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