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

Authors :
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
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
Source :
Nature genetics, 14 (4
Publication Year :
1996

Abstract

Hallervorden-Spatz syndrome (HSS) (OMIM<br />Journal Article<br />Research Support, Non-U.S. Gov't<br />Research Support, U.S. Gov't, P.H.S.<br />info:eu-repo/semantics/published

Details

Database :
OAIster
Journal :
Nature genetics, 14 (4
Notes :
No full-text files, English
Publication Type :
Electronic Resource
Accession number :
edsoai.ocn764603458
Document Type :
Electronic Resource