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

Pub. Date : 2005 Jul

PMID : 15871139






1 Functional Relationships(s)
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Protein Name
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1 Biotin-responsive basal ganglia disease maps to 2q36.3 and is due to mutations in SLC19A3. Biotin solute carrier family 19 member 3 Homo sapiens