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XB-GENEPAGE-6464684
Papers associated with fbrsl1
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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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