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Q37292864-5E21F4D3-BB57-4503-B8E5-AB283CC1ED68
Q37292864-5E21F4D3-BB57-4503-B8E5-AB283CC1ED68
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37292864-5E21F4D3-BB57-4503-B8E5-AB283CC1ED68
Treatable Leigh-like encephalopathy presenting in adolescence.
P2860
Q37292864-5E21F4D3-BB57-4503-B8E5-AB283CC1ED68
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37292864-5E21F4D3-BB57-4503-B8E5-AB283CC1ED68
rank
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Statement
wasDerivedFrom
db092864d327c01735ac5d106c4fa43ba111b0ee
P2860
Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome.