Titre :
  • TM4SF10 gene sequencing in XLMR patients identifies common polymorphisms but no disease-associated mutation
Auteur : Hobertus, Christiane ; Kooy, F. ; Gecz, J. ; Abramowicz, Marc ; Holinski-Feder, Elke ; Schwartz, C. ; Christophe, Daniel
Informations sur la publication : BMC medical genetics, 5, 22
Statut de publication : Publié, 2004
Sujet CREF : Biologie moléculaire
Mots-clés MeSH : 3' Untranslated Regions -- chemistry
Exons
Female
Genetic Predisposition to Disease
Humans
Male
Membrane Proteins -- genetics
Mental Retardation, X-Linked -- genetics
Mutation
Nerve Tissue Proteins -- genetics
Polymerase Chain Reaction
Polymorphism, Single Nucleotide
Sequence Analysis, DNA
Note : Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.
SCOPUS: ar.j
Langue :
  • Anglais
Identificateurs : urn:issn:1471-2350 
info:doi/10.1186/1471-2350-5-22
info:pii/1471-2350-5-22
info:pmid/15345028
info:pmcid/PMC517934
cd-0069