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Q45057319-61F86A80-B01C-46CB-93C2-3EB2DF54FCA1
Q45057319-61F86A80-B01C-46CB-93C2-3EB2DF54FCA1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45057319-61F86A80-B01C-46CB-93C2-3EB2DF54FCA1
P4HA1 mutations cause a unique congenital disorder of connective tissue involving tendon, bone, muscle and the eye.
P2860
Q45057319-61F86A80-B01C-46CB-93C2-3EB2DF54FCA1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45057319-61F86A80-B01C-46CB-93C2-3EB2DF54FCA1
rank
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type
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Statement
wasDerivedFrom
4dab5a1cc3b3ca95523348e9251cae8d77f70d17
P2860
Loss of assembly of the main basement membrane collagen, type IV, but not fibril-forming collagens and embryonic death in collagen prolyl 4-hydroxylase I null mice