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Q46268668-C9A766E9-87FF-4726-AA59-2D399FDB5CA2
Q46268668-C9A766E9-87FF-4726-AA59-2D399FDB5CA2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46268668-C9A766E9-87FF-4726-AA59-2D399FDB5CA2
Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome.
P2860
Q46268668-C9A766E9-87FF-4726-AA59-2D399FDB5CA2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46268668-C9A766E9-87FF-4726-AA59-2D399FDB5CA2
rank
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type
BestRank
Statement
wasDerivedFrom
d63a53c4a67780c57dd301f509384471c724cc6d
P2860
A novel mutation in the thiamine responsive megaloblastic anaemia gene SLC19A2 in a patient with deficiency of respiratory chain complex I