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Q28306581-33A33460-1DE2-406C-A942-F34D3D00B51A
Q28306581-33A33460-1DE2-406C-A942-F34D3D00B51A
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Statement
http://www.wikidata.org/entity/statement/Q28306581-33A33460-1DE2-406C-A942-F34D3D00B51A
Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects
P2860
Q28306581-33A33460-1DE2-406C-A942-F34D3D00B51A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28306581-33A33460-1DE2-406C-A942-F34D3D00B51A
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wasDerivedFrom
3c3ac2adb58eef0525aa094cd9b3a4bfc6fe8d79
P2860
Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetry.