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Q39610283-65DF211D-DE89-4B5A-9194-5F0D645EE0EC
Q39610283-65DF211D-DE89-4B5A-9194-5F0D645EE0EC
BestRank
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http://www.wikidata.org/entity/statement/Q39610283-65DF211D-DE89-4B5A-9194-5F0D645EE0EC
Genetic and epigenetic methylation defects and implication of the ERMN gene in autism spectrum disorders.
P2860
Q39610283-65DF211D-DE89-4B5A-9194-5F0D645EE0EC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39610283-65DF211D-DE89-4B5A-9194-5F0D645EE0EC
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type
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wasDerivedFrom
18b4b540552d3eeaae3128b2906e61080c6ae229
P2860
A new syndrome: progressive familial infantile cerebral dysfunction associated with an unusual urinary substance.