Condition: Factor Xiii, A Subunit, Deficiency Of


rs121913064 in F13A1 gene and Factor Xiii, A Subunit, Deficiency Of PMID 24329762 2014 Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations.

PMID 20179087 2010 Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function.

PMID 24286209 2014 Severe congenital factor XIII deficiency caused by novel W187X and G273V mutations in the F13A gene; diagnosis and classification according to the ISTH/SSC guidelines.

PMID 1353995 1992 Identification of a point mutation in factor XIII A subunit deficiency.

PMID 24889649 2014 Eight novel F13A1 gene missense mutations in patients with mild FXIII deficiency: in silico analysis suggests changes in FXIII-A subunit structure/function.

PMID 27363989 2016 Coagulation Factor XIIIA Subunit Missense Mutations Affect Structure and Function at the Various Steps of Factor XIII Action.

PMID 28520207 2017 Comparison of F13A1 gene mutations in 73 patients treated with recombinant FXIII-A2.

PMID 24118344 2014 Factor XIII deficiency: complete phenotypic characterization of two cases with novel causative mutations.

PMID 8547636 1996 Four novel mutations in deficiency of coagulation factor XIII: consequences to expression and structure of the A-subunit.

PMID 11167856 2001 Two novel and one recurrent missense mutation in the factor XIII A gene in two Dutch patients with factor XIII deficiency.

rs369187276 in F13A1;MIR5683 gene and Factor Xiii, A Subunit, Deficiency Of PMID 24889649 2014 Eight novel F13A1 gene missense mutations in patients with mild FXIII deficiency: in silico analysis suggests changes in FXIII-A subunit structure/function.

PMID 24286209 2014 Severe congenital factor XIII deficiency caused by novel W187X and G273V mutations in the F13A gene; diagnosis and classification according to the ISTH/SSC guidelines.

PMID 20179087 2010 Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function.

PMID 1353995 1992 Identification of a point mutation in factor XIII A subunit deficiency.

PMID 27363989 2016 Coagulation Factor XIIIA Subunit Missense Mutations Affect Structure and Function at the Various Steps of Factor XIII Action.

PMID 24329762 2014 Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations.

rs138754417 in MIR5683;F13A1 gene and Factor Xiii, A Subunit, Deficiency Of PMID 24889649 2014 Eight novel F13A1 gene missense mutations in patients with mild FXIII deficiency: in silico analysis suggests changes in FXIII-A subunit structure/function.

PMID 1353995 1992 Identification of a point mutation in factor XIII A subunit deficiency.

PMID 27363989 2016 Coagulation Factor XIIIA Subunit Missense Mutations Affect Structure and Function at the Various Steps of Factor XIII Action.

PMID 20179087 2010 Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function.

PMID 24286209 2014 Severe congenital factor XIII deficiency caused by novel W187X and G273V mutations in the F13A gene; diagnosis and classification according to the ISTH/SSC guidelines.

PMID 24329762 2014 Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations.