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PubMed (OMIM) for id: 56776
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Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disability.
Am J Hum Genet. 2014 Dec 4;95(6):721-8. doi: 10.1016/j.ajhg.2014.10.016.
Am J Hum Genet. 2014.
PMID: 25480035
Free PMC article.
Formin-2, polyploidy, hypofertility and positioning of the meiotic spindle in mouse oocytes.
Leader B, Lim H, Carabatsos MJ, Harrington A, Ecsedy J, Pellman D, Maas R, Leder P.
Leader B, et al.
Nat Cell Biol. 2002 Dec;4(12):921-8. doi: 10.1038/ncb880.
Nat Cell Biol. 2002.
PMID: 12447394
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Formin-2, a novel formin homology protein of the cappuccino subfamily, is highly expressed in the developing and adult central nervous system.
Leader B, Leder P.
Leader B, et al.
Mech Dev. 2000 May;93(1-2):221-31. doi: 10.1016/s0925-4773(00)00276-8.
Mech Dev. 2000.
PMID: 10781961
Free article.
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