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Summary Attributions Wiki
XB-MORPHOLINO-22249065

Attributions for fbrsl1 E1/I1

Papers


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. May 18, 2020;                           


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