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4116971
4116971
https://w3id.org/oc/corpus/br/4116971
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
P3181
eb422eb27ab61afb147ab2c8b6f13d3cab9812e4
P3181
Q28188363-DBEF8298-704E-4BB6-961B-A39D9CF9FD40
P3181
4116971
https://w3id.org/oc/corpus/br/4116971