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- NP837201.RAykjY62-IzxeS48OOh_qU7mBJ-WX9mv3Fvq6d0eN7Eew130_assertion type Assertion NP837201.RAykjY62-IzxeS48OOh_qU7mBJ-WX9mv3Fvq6d0eN7Eew130_head.
- NP837201.RAykjY62-IzxeS48OOh_qU7mBJ-WX9mv3Fvq6d0eN7Eew130_assertion description "[Heterozygous missense mutations in PITX3 have been reported in patients with autosomal dominant congenital cataract and anterior segment (ocular) mesenchymal dysgenesis (ASMD) whereas homozygous missense mutations have been found in patients with microphthalmia and neurological impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837201.RAykjY62-IzxeS48OOh_qU7mBJ-WX9mv3Fvq6d0eN7Eew130_provenance.
- NP837201.RAykjY62-IzxeS48OOh_qU7mBJ-WX9mv3Fvq6d0eN7Eew130_assertion evidence source_evidence_literature NP837201.RAykjY62-IzxeS48OOh_qU7mBJ-WX9mv3Fvq6d0eN7Eew130_provenance.
- NP837201.RAykjY62-IzxeS48OOh_qU7mBJ-WX9mv3Fvq6d0eN7Eew130_assertion SIO_000772 22223473 NP837201.RAykjY62-IzxeS48OOh_qU7mBJ-WX9mv3Fvq6d0eN7Eew130_provenance.
- NP837201.RAykjY62-IzxeS48OOh_qU7mBJ-WX9mv3Fvq6d0eN7Eew130_assertion wasDerivedFrom befree-20140225 NP837201.RAykjY62-IzxeS48OOh_qU7mBJ-WX9mv3Fvq6d0eN7Eew130_provenance.
- NP837201.RAykjY62-IzxeS48OOh_qU7mBJ-WX9mv3Fvq6d0eN7Eew130_assertion wasGeneratedBy ECO_0000203 NP837201.RAykjY62-IzxeS48OOh_qU7mBJ-WX9mv3Fvq6d0eN7Eew130_provenance.