Recurrent European missense mutation in the F12 gene in a British family with type III hereditary angioedema
スポンサーリンク
概要
- 論文の詳細を見る
- 2009-10-01
著者
-
Mcgrath John
St John's Institute Of Dermatology 9th Floor Tower Wing Guy's Hospital
-
Mcgrath John
St John's Institute Of Dermatology King's College London
-
NAGY Nikoletta
St John's Institute of Dermatology, King's College London
-
GREAVES Malcolm
Department of Dermatology, Poole General Hospital
-
TANAKA Akio
St John's Institute of Dermatology, King's College London
-
GRATTAN Clive
St John's Institute of Dermatology, The Guy's and St Thomas' NHS Foundation Trust
-
Grattan Clive
St John's Institute Of Dermatology The Guy's And St Thomas' Nhs Foundation Trust
-
Tanaka Akio
St John's Institute Of Dermatology King's College London
-
Nagy Nikoletta
St John's Institute Of Dermatology King's College London
-
Greaves Malcolm
Department Of Dermatology Poole General Hospital
関連論文
- Rapid diagnosis of lipoid proteinosis using an anti-extracellular matrix protein 1 (ECM1) antibody
- Schopf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A
- Recurrent European missense mutation in the F12 gene in a British family with type III hereditary angioedema