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Biotin-responsive basal ganglia disease maps to 2q36.3 and is due to mutations in SLC19A3.

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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
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PubType: Academic Journal
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  Data: Biotin-responsive basal ganglia disease maps to 2q36.3 and is due to mutations in SLC19A3.
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  Data: <searchLink fieldCode="JN" term="%220370475%22">American journal of human genetics</searchLink> [Am J Hum Genet] 2005 Jul; Vol. 77 (1), pp. 16-26. <i>Date of Electronic Publication: </i>2005 May 03.
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  Data: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Cell+Press%22">Cell Press </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>0370475 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Print <i>ISSN: </i>0002-9297 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200029297%22">00029297 </searchLink><i>NLM ISO Abbreviation: </i>Am J Hum Genet <i>Subsets: </i>MEDLINE
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      – Type: doi
        Value: 10.1086/431216
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      – Code: eng
        Text: English
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      – TitleFull: Biotin-responsive basal ganglia disease maps to 2q36.3 and is due to mutations in SLC19A3.
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            NameFull: Zeng WQ
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            NameFull: Al-Yamani E
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            NameFull: Acierno JS Jr
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              Text: 2005 Jul
              Type: published
              Y: 2005
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              Value: 77
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            – TitleFull: American journal of human genetics
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