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Q37619281-02482FBF-1013-4F4F-8549-2FBC7C95E6BF
Q37619281-02482FBF-1013-4F4F-8549-2FBC7C95E6BF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37619281-02482FBF-1013-4F4F-8549-2FBC7C95E6BF
Allelic heterogeneity contributes to variability in ocular dysgenesis, myopathy and brain malformations caused by Col4a1 and Col4a2 mutations.
P2860
Q37619281-02482FBF-1013-4F4F-8549-2FBC7C95E6BF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37619281-02482FBF-1013-4F4F-8549-2FBC7C95E6BF
rank
NormalRank
type
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wasDerivedFrom
8f97df45f5eb7587b9918a9a9945279bdcbe9a71
P2860
Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities