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Summary Expression Phenotypes Gene Literature (2) GO Terms (0) Nucleotides (135) Proteins (27) Interactants (78) Wiki
XB--987495

Papers associated with auts2 (and Disease Ontology)



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De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome., Ufartes R, Berger H, Till K, Salinas G, Sturm M, Altmüller J, Nürnberg P, Thiele H, Funke R, Apeshiotis N, Langen H, Wollnik B, Borchers A, Pauli S., Hum Genet. November 1, 2020; 139 (11): 1363-1379.                                        

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