FOXI1
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| FOXI1 | |
|---|---|
| Identifiers | |
| Symbol | FOXI1 |
| Alt. symbols | FKHL10 |
| Entrez | 2299 |
| HUGO | 3815 |
| OMIM | 601093 |
| RefSeq | NM_144769 |
| Other data | |
| Locus | Chr. 5 q34 |
FOXI1 is a human gene.
It can be associated with enlarged vestibular aqueduct.[1]
[edit] See also
[edit] References
- ^ Yang T, Vidarsson H, Rodrigo-Blomqvist S, Rosengren SS, Enerback S, Smith RJ (June 2007). "Transcriptional control of SLC26A4 is involved in Pendred syndrome and nonsyndromic enlargement of vestibular aqueduct (DFNB4)". Am. J. Hum. Genet. 80 (6): 1055–63. doi:10.1086/518314. PMC 1867094. PMID 17503324. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1867094.
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