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TM4SF10 gene sequencing in XLMR patients identifies common polymorphisms but no disease-associated mutation

par Hobertus, Christiane ;Kooy, F.;Gecz, J.;Abramowicz, Marc ;Holinski-Feder, Elke;Schwartz, C.;Christophe, Daniel
Référence BMC medical genetics, 5, 22
Publication Publié, 2004

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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
MeSH keywords:	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 générale:	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:scp/26444569295
	info:pmid/15345028
	PMC517934
	cd-0069