Bibliographic Details
| Title: |
Biotin-responsive basal ganglia disease maps to 2q36.3 and is due to mutations in SLC19A3. |
| Authors: |
Zeng WQ; Molecular Neurogenetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, Charlestown, MA 02129-2000, USA., Al-Yamani E, Acierno JS Jr, Slaugenhaupt S, Gillis T, MacDonald ME, Ozand PT, Gusella JF |
| Source: |
American journal of human genetics [Am J Hum Genet] 2005 Jul; Vol. 77 (1), pp. 16-26. Date of Electronic Publication: 2005 May 03. |
| Publication Type: |
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. |
| Journal Info: |
Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0002-9297 (Print) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE |
| Database: |
MEDLINE Ultimate |
