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Q37098005-AB242363-3E19-43ED-815A-37BE86B7D9C2
Q37098005-AB242363-3E19-43ED-815A-37BE86B7D9C2
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Statement
http://www.wikidata.org/entity/statement/Q37098005-AB242363-3E19-43ED-815A-37BE86B7D9C2
Mutations in LAMB2 causing a severe form of synaptic congenital myasthenic syndrome.
P2860
Q37098005-AB242363-3E19-43ED-815A-37BE86B7D9C2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37098005-AB242363-3E19-43ED-815A-37BE86B7D9C2
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wasDerivedFrom
64b466f228527fbe7b73314fa86d9318389e9daf
P2860
Transgenic isolation of skeletal muscle and kidney defects in laminin beta2 mutant mice: implications for Pierson syndrome