A novel complex insertion-deletion mutation in the FOXC2 gene in a Japanese patient with Lymphedema-Distichiasis Syndrome
Identifieur interne : 003C84 ( Main/Exploration ); précédent : 003C83; suivant : 003C85A novel complex insertion-deletion mutation in the FOXC2 gene in a Japanese patient with Lymphedema-Distichiasis Syndrome
Auteurs : Munenari Itoh [Japon] ; Hidemi Nakagawa [Japon]Source :
- EJD. European journal of dermatology [ 1167-1122 ] ; 2013.
Descripteurs français
- Pascal (Inist)
- Wicri :
English descriptors
- KwdEn :
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PascalFrancis, to step Corpus: 000029
- to stream PascalFrancis, to step Curation: 000926
- to stream PascalFrancis, to step Checkpoint: 000042
- to stream Main, to step Merge: 003C95
- to stream Main, to step Curation: 003C84
Le document en format XML
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<term>Deletion</term>
<term>Dermatology</term>
<term>Distichiasis</term>
<term>Gene</term>
<term>Genetics</term>
<term>Human</term>
<term>Insertion mutation</term>
<term>Japan</term>
<term>Japanese</term>
<term>Lymphedema</term>
<term>Patient</term>
<term>Syndrome</term>
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<term>Lymphoedème</term>
<term>Distichiasis</term>
<term>Complexité</term>
<term>Mutation insertion</term>
<term>Gène</term>
<term>Homme</term>
<term>Génétique</term>
<term>Malade</term>
<term>Japon</term>
<term>Japonais</term>
<term>Syndrome</term>
<term>Dermatologie</term>
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