Homo sapiens mRNA; cDNA DKFZp686J1293 (from clone DKFZp686J1293)

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A Comprehensive Overview of NF1 Mutations in Iranian Patients. [Neuromolecular Med. 2024]
A Comprehensive Overview of NF1 Mutations in Iranian Patients.
Savad S, Modarressi MH, Younesi S, Seifi-Alan M, Samadaian N, Masoomy M, Dianatpour M, Norouzi S, Amidi S, Boroumand A, et al. Neuromolecular Med. 2024 Jul 2; 26(1):28. Epub 2024 Jul 2.
MEK-SHP2 inhibition prevents tibial pseudarthrosis caused by NF1 loss in Schwann cells and skeletal stem/progenitor cells. [Sci Transl Med. 2024]
MEK-SHP2 inhibition prevents tibial pseudarthrosis caused by NF1 loss in Schwann cells and skeletal stem/progenitor cells.
Perrin S, Protic S, Bretegnier V, Laurendeau I, de Lageneste OD, Panara N, Ruckebusch O, Luka M, Masson C, Maillard T, et al. Sci Transl Med. 2024 Jun 26; 16(753):eadj1597. Epub 2024 Jun 26.
Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes. [Hum Genet. 2024]
Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes.
Tritto V, Bettinaglio P, Mangano E, Cesaretti C, Marasca F, Castronovo C, Bordoni R, Battaglia C, Saletti V, Ranzani V, et al. Hum Genet. 2024 Jun; 143(6):775-795. Epub 2024 Jun 14.

RefSeq alternative splicing
See 3 reference mRNA sequence splice variants for the NF1 gene.

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Nucleotide