• Citer

Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13.

par Taylor, T D;Litt, Madeleine;Kramer, P;Pandolfo, Massimo ;Angelini, L;Nardocci, N;Davis, Stacy;Pineda, M;Hattori, Hidenori;Flett, P J;Cilio, M R;Bertini, E;Hayflick, S J
Référence Nature genetics, 14, 4, page (479-481)
Publication Publié, 1996-12

Article révisé par les pairs

• Détails
• Contenu

Titre:	Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13.
Auteur:	Taylor, T D; Litt, Madeleine; Kramer, P; Pandolfo, Massimo; Angelini, L; Nardocci, N; Davis, Stacy; Pineda, M; Hattori, Hidenori; Flett, P J; Cilio, M R; Bertini, E; Hayflick, S J
Informations sur la publication:	Nature genetics, 14, 4, page (479-481)
Statut de publication:	Publié, 1996-12
Sujet CREF:	Sciences bio-médicales et agricoles
MeSH keywords:	Chromosome Mapping
	Chromosomes, Human, Pair 20
	Consanguinity
	Female
	Genetic Markers
	Homozygote
	Humans
	Linkage (Genetics)
	Male
	Pantothenate Kinase-Associated Neurodegeneration -- genetics
	Pedigree
Note générale:	Journal Article
	Research Support, Non-U.S. Gov't
	Research Support, U.S. Gov't, P.H.S.
Langue:	Anglais
Identificateurs:	urn:issn:1061-4036
	info:doi/10.1038/ng1296-479
	info:pmid/8944032