Similar articles

• Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutations.

  Castaman G, Giacomelli SH, Duga S, Rodeghiero F. Castaman G, et al. Haemophilia. 2008 May;14(3):630-3. doi: 10.1111/j.1365-2516.2008.01692.x. Epub 2008 Apr 3. Haemophilia. 2008. PMID: 18393984 No abstract available.
• Three cases of abnormal fibrinogens: sumperk (Bbeta His67Leu), Unicov (Bbeta Gly414Ser), and Brno (gammaArg275His).

  Kotlín R, Reicheltová Z, Sobotková A, Suttnar J, Salaj P, Pospísilová D, Smejkal P, Chrastinová L, Dyr JE. Kotlín R, et al. Thromb Haemost. 2008 Dec;100(6):1199-200. Thromb Haemost. 2008. PMID: 19132250 No abstract available.
• A case of congenital afibrinogenemia: fibrinogen Hakata, a novel nonsense mutation of the fibrinogen gamma-chain gene.

  Iida H, Ishii E, Nakahara M, Urata M, Wakiyama M, Kurihara M, Watanabe K, Kai T, Ihara K, Kinoshita S, Hamasaki N. Iida H, et al. Thromb Haemost. 2000 Jul;84(1):49-53. Thromb Haemost. 2000. PMID: 10928469
• The molecular basis of inherited afibrinogenaemia.

  Neerman-Arbez M. Neerman-Arbez M. Thromb Haemost. 2001 Jul;86(1):154-63. Thromb Haemost. 2001. PMID: 11487003 Review.
• A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream.

  Robert-Ebadi H, de Moerloose P, El Khorassani M, El Khattab M, Neerman-Arbez M. Robert-Ebadi H, et al. Blood Coagul Fibrinolysis. 2009 Jul;20(5):385-7. doi: 10.1097/MBC.0b013e328329f2a0. Blood Coagul Fibrinolysis. 2009. PMID: 19417632 Review.