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Atypical Cogan syndrome: a case report.
J Med Case Rep. 2024 Nov 14;18(1):551. doi: 10.1186/s13256-024-04904-6.
J Med Case Rep. 2024.
PMID: 39543746
Free PMC article.
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. Among authors: el khattab m.
Blood Coagul Fibrinolysis. 2009 Jul;20(5):385-7. doi: 10.1097/MBC.0b013e328329f2a0.
Blood Coagul Fibrinolysis. 2009.
PMID: 19417632
Review.
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