Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, … - Full text - MIT Libraries
LM Peters, DW Anderson, AJ Griffith, KM Grundfast, … - Human Molecular Genetics, 2002 - hmg.oupjournals.org
... amino acid sequence alignment of TFCP2L3 compared with TFCP2, TFCP2L2 and ... by mutations
of genes encoding the transcription factors PAX3 (Waardenburg syndrome ...
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Deafness Genes and Their Diagnostic Applications - Full text - MIT Libraries
KCG Van Camp - Audiol Neurootol, 2004 - content.karger.com
... Interestingly, PAX3 and SOX10 transactivate MITF, and mutations in either of 2 ... to
the family of transcription factor cellular promoter 2 (TFCP2) pro- teins ...
Web Search - content.karger.com

HUMAN NONSYNDROMIC SENSORINEURAL DEAFNESS* - Full text - MIT Libraries
TB Friedman, AJ Griffith - Annual Review of Genomics and Human Genetics, 2003 - nutr.annualreviews.org
Annual Reviews tagline graphic, ...
Cited by 20 - Web Search - genom.annualreviews.org - genom.annualreviews.org - ncbi.nlm.nih.gov - all 5 versions »