[HTML][HTML] SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE
Hereditary angioedema with C1 Inhibitor deficiency (C1-INH-HAE) is caused by a
constellation of variants of the SERPING1 gene (n= 809; 1,494 pedigrees), accounting for …
constellation of variants of the SERPING1 gene (n= 809; 1,494 pedigrees), accounting for …
[PDF][PDF] SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE
C Drouet, A López-Lera, A Ghannam… - researchgate.net
Drouet et al. SERPING1 Variants and C-INH Expression benign variants could contribute as
disease modifiers. Gonadal mosaicism in C1-INH-HAE is rare and must be distinguished …
disease modifiers. Gonadal mosaicism in C1-INH-HAE is rare and must be distinguished …
SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE
C Drouet, A López-Lera, A Ghannam… - Frontiers in …, 2022 - pubmed.ncbi.nlm.nih.gov
Hereditary angioedema with C1 Inhibitor deficiency (C1-INH-HAE) is caused by a
constellation of variants of the SERPING1 gene (n= 809; 1,494 pedigrees), accounting for …
constellation of variants of the SERPING1 gene (n= 809; 1,494 pedigrees), accounting for …
SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE
C Drouet, A López-Lera, A Ghannam… - Frontiers in …, 2022 - cir.nii.ac.jp
抄録< jats: p> Hereditary angioedema with C1 Inhibitor deficiency (C1-INH-HAE) is caused
by a constellation of variants of the< jats: italic> SERPING1</jats: italic> gene (< jats: italic> …
by a constellation of variants of the< jats: italic> SERPING1</jats: italic> gene (< jats: italic> …
SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE
C Drouet, A López-Lera, A Ghannam… - 2022 - med.muni.cz
Hereditary angioedema with C1 Inhibitor deficiency (C1-INH-HAE) is caused by a
constellation of variants of the SERPING1 gene (n= 809; 1,494 pedigrees), accounting for …
constellation of variants of the SERPING1 gene (n= 809; 1,494 pedigrees), accounting for …
SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE.
C Drouet, A López-Lera, A Ghannam… - Frontiers in …, 2022 - europepmc.org
Hereditary angioedema with C1 Inhibitor deficiency (C1-INH-HAE) is caused by a
constellation of variants of the SERPING1 gene (n= 809; 1,494 pedigrees), accounting for …
constellation of variants of the SERPING1 gene (n= 809; 1,494 pedigrees), accounting for …
[PDF][PDF] SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE
C Drouet, A López-Lera, A Ghannam… - Frontiers in …, 2022 - hal.univ-grenoble-alpes.fr
Hereditary angioedema with C1 Inhibitor deficiency (C1-INH-HAE) is caused by a
constellation of variants of the SERPING1 gene (n= 809; 1,494 pedigrees), accounting for …
constellation of variants of the SERPING1 gene (n= 809; 1,494 pedigrees), accounting for …
[PDF][PDF] SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE
C Drouet, A López-Lera, A Ghannam… - academia.edu
Drouet et al. SERPING1 Variants and C-INH Expression benign variants could contribute as
disease modifiers. Gonadal mosaicism in C1-INH-HAE is rare and must be distinguished …
disease modifiers. Gonadal mosaicism in C1-INH-HAE is rare and must be distinguished …
[HTML][HTML] SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE
C Drouet, A López-Lera, A Ghannam… - Frontiers in …, 2022 - ncbi.nlm.nih.gov
Hereditary angioedema with C1 Inhibitor deficiency (C1-INH-HAE) is caused by a
constellation of variants of the SERPING1 gene (n= 809; 1,494 pedigrees), accounting for …
constellation of variants of the SERPING1 gene (n= 809; 1,494 pedigrees), accounting for …
SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE
C Drouet, A López-Lera, A Ghannam… - C1 Inhibitor …, 2022 - books.google.com
Drouet et al. SERPING1 Variants and C-INH Expression benign variants could contribute as
disease modifiers. Gonadal mosaicism in C1-INH-HAE is rare and must be distinguished …
disease modifiers. Gonadal mosaicism in C1-INH-HAE is rare and must be distinguished …