Title : Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome.

Pub. Date : 2013 Mar

PMID : 23423671






1 Functional Relationships(s)
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1 Our data shows that SLC19A3 is a new candidate for mutation screening in patients with Leigh syndrome, who might benefit from high doses of thiamine and/or biotin. Biotin solute carrier family 19 member 3 Homo sapiens