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Q51933512-1C876083-F360-45EF-B8AE-3AFC77C70854
Q51933512-1C876083-F360-45EF-B8AE-3AFC77C70854
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51933512-1C876083-F360-45EF-B8AE-3AFC77C70854
Two novel mutations in SLC6A8 cause creatine transporter defect and distinctive X-linked mental retardation in two unrelated Dutch families.
P2860
Q51933512-1C876083-F360-45EF-B8AE-3AFC77C70854
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51933512-1C876083-F360-45EF-B8AE-3AFC77C70854
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Statement
wasDerivedFrom
f33c2bc76cce63d6d7a8cf175152c9cb50e6a661
P2860
X-linked creatine deficiency syndrome: a novel mutation in creatine transporter gene SLC6A8.