Functional and splicing defect analysis of 23 ACVRL1 mutations in a cohort of patients affected by Hereditary Hemorrhagic Telangiectasia (Q28116278)
Jump to navigation
Jump to search
scientific journal article
Language | Label | Description | Also known as |
---|---|---|---|
English | Functional and splicing defect analysis of 23 ACVRL1 mutations in a cohort of patients affected by Hereditary Hemorrhagic Telangiectasia |
scientific journal article |
Statements
2 references
Functional and splicing defect analysis of 23 ACVRL1 mutations in a cohort of patients affected by Hereditary Hemorrhagic Telangiectasia (English)
2 references
Ferdos Alaa El Din
2 references
Sylvie Patri
2 references
Vincent Thoreau
2 references
Montserrat Rodriguez-Ballesteros
2 references
Raghida Abou Merhi
2 references
Alain Kitzis
2 references
2 references
10
2 references
7
2 references
e0132111
2 references
15 July 2015
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
2 references