Loss‐of‐function variants in <i>NFIA</i> provide further support that <i>NFIA</i> is a critical gene in 1p32‐p31 deletion syndrome: A four patient series
Anya Revah‐Politi(A&G Pharmaceutical (United States)), Kwame Anyane‐Yeboa(Columbia University Irving Medical Center), David B. Goldstein(Electronic BioSciences (United States)), John Pappas(New York University), Mythily Ganapathi(Columbia University Irving Medical Center), Alejandro Iglesias(Columbia University Irving Medical Center), Vimla S. Aggarwal(Columbia University Irving Medical Center), Megan T. Cho, Parisa Hemati(Columbia University Irving Medical Center), Slavé Petrovski(AstraZeneca (United Kingdom)), Louise Bier(Columbia University Irving Medical Center), Jane Juusola, Ashley Wilson(Center for Infectious Disease Research)
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