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Q41898877-B2FAB3CC-D961-4835-AF87-350C8EF9E08B
Q41898877-B2FAB3CC-D961-4835-AF87-350C8EF9E08B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41898877-B2FAB3CC-D961-4835-AF87-350C8EF9E08B
Whole exome sequencing reveals compound heterozygous mutations in SLC19A3 causing biotin-thiamine responsive basal ganglia disease.
P478
Q41898877-B2FAB3CC-D961-4835-AF87-350C8EF9E08B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41898877-B2FAB3CC-D961-4835-AF87-350C8EF9E08B
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
c7fa259b0fe76d5bfa2d7a930bc232eaf1475dbf
P478
1
http://www.w3.org/2001/XMLSchema#string