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- NP455149.RAyjt07wL5_CzkBaN7yQN0TL5pdQobDEaNW0FrIGOUrDU130_assertion type Assertion NP455149.RAyjt07wL5_CzkBaN7yQN0TL5pdQobDEaNW0FrIGOUrDU130_head.
- NP455149.RAyjt07wL5_CzkBaN7yQN0TL5pdQobDEaNW0FrIGOUrDU130_assertion description "[We identified a homozygous missense mutation (c.196G-->T) in fibroblast growth factor 3 (FGF3) in 21 affected individuals from a large extended consanguineous Saudi family, phenotypically characterized by autosomal recessive syndromic congenital sensorineural deafness, microtia and microdontia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP455149.RAyjt07wL5_CzkBaN7yQN0TL5pdQobDEaNW0FrIGOUrDU130_provenance.
- NP455149.RAyjt07wL5_CzkBaN7yQN0TL5pdQobDEaNW0FrIGOUrDU130_assertion evidence source_evidence_literature NP455149.RAyjt07wL5_CzkBaN7yQN0TL5pdQobDEaNW0FrIGOUrDU130_provenance.
- NP455149.RAyjt07wL5_CzkBaN7yQN0TL5pdQobDEaNW0FrIGOUrDU130_assertion SIO_000772 18701883 NP455149.RAyjt07wL5_CzkBaN7yQN0TL5pdQobDEaNW0FrIGOUrDU130_provenance.
- NP455149.RAyjt07wL5_CzkBaN7yQN0TL5pdQobDEaNW0FrIGOUrDU130_assertion wasDerivedFrom befree-20140225 NP455149.RAyjt07wL5_CzkBaN7yQN0TL5pdQobDEaNW0FrIGOUrDU130_provenance.
- NP455149.RAyjt07wL5_CzkBaN7yQN0TL5pdQobDEaNW0FrIGOUrDU130_assertion wasGeneratedBy ECO_0000203 NP455149.RAyjt07wL5_CzkBaN7yQN0TL5pdQobDEaNW0FrIGOUrDU130_provenance.