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- NP463389.RAvKfo_X-47wRU0-Ga1850rhVlae8MIWcT-Sc0gv199sc130_assertion type Assertion NP463389.RAvKfo_X-47wRU0-Ga1850rhVlae8MIWcT-Sc0gv199sc130_head.
- NP463389.RAvKfo_X-47wRU0-Ga1850rhVlae8MIWcT-Sc0gv199sc130_assertion wasGeneratedBy ECO_0000203 NP463389.RAvKfo_X-47wRU0-Ga1850rhVlae8MIWcT-Sc0gv199sc130_provenance.
- NP463389.RAvKfo_X-47wRU0-Ga1850rhVlae8MIWcT-Sc0gv199sc130_assertion wasDerivedFrom befree-20150227 NP463389.RAvKfo_X-47wRU0-Ga1850rhVlae8MIWcT-Sc0gv199sc130_provenance.
- NP463389.RAvKfo_X-47wRU0-Ga1850rhVlae8MIWcT-Sc0gv199sc130_assertion SIO_000772 17236141 NP463389.RAvKfo_X-47wRU0-Ga1850rhVlae8MIWcT-Sc0gv199sc130_provenance.
- NP463389.RAvKfo_X-47wRU0-Ga1850rhVlae8MIWcT-Sc0gv199sc130_assertion evidence source_evidence_literature NP463389.RAvKfo_X-47wRU0-Ga1850rhVlae8MIWcT-Sc0gv199sc130_provenance.
- NP463389.RAvKfo_X-47wRU0-Ga1850rhVlae8MIWcT-Sc0gv199sc130_assertion description "[Polyalanine expansions in HOXD13 cause synpolydactyly, whereas amino acid substitutions in the homeodomain are associated with brachydactyly types D and E. We describe two large Han Chinese families with different limb malformations, one with syndactyly type V and the other with limb features overlapping brachydactyly types A4, D, and E and mild syndactyly of toes 2 and 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463389.RAvKfo_X-47wRU0-Ga1850rhVlae8MIWcT-Sc0gv199sc130_provenance.