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Q58703107-182EAEBE-D049-4EFB-8279-8B12694F54C7
Q58703107-182EAEBE-D049-4EFB-8279-8B12694F54C7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58703107-182EAEBE-D049-4EFB-8279-8B12694F54C7
A novel MFSD8 mutation in a Russian patient with neuronal ceroid lipofuscinosis type 7: a case report
P2860
Q58703107-182EAEBE-D049-4EFB-8279-8B12694F54C7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58703107-182EAEBE-D049-4EFB-8279-8B12694F54C7
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type
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Statement
wasDerivedFrom
0e773974bc9b9e397d190bd7a9d4d51d538f636b
P2860
Clinico-pathological manifestations of variant late infantile neuronal ceroid lipofuscinosis (vLINCL) caused by a novel mutation in MFSD8 gene.