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Q47701991-B643F73F-7E4C-4701-8157-AEDDCB310710
Q47701991-B643F73F-7E4C-4701-8157-AEDDCB310710
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47701991-B643F73F-7E4C-4701-8157-AEDDCB310710
Novel mutations of CLCN7 cause autosomal dominant osteopetrosis type II (ADOII) and intermediate autosomal recessive osteopetrosis (ARO) in seven Chinese families.
P407
Q47701991-B643F73F-7E4C-4701-8157-AEDDCB310710
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47701991-B643F73F-7E4C-4701-8157-AEDDCB310710
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type
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P407
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