Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment
- 1 May 1998
- journal article
- letter
- Published by Springer Science and Business Media LLC in Nature Genetics
- Vol. 19 (1), 60-62
- https://doi.org/10.1038/ng0598-60
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Mapping of the α-Tectorin Gene (TECTA) to Mouse Chromosome 9 and Human Chromosome 11: A Candidate for Human Autosomal Dominant Nonsyndromic DeafnessGenomics, 1998
- The Mouse TectorinsPublished by Elsevier BV ,1997
- A Sperm Membrane Protein That Binds in a Species-specific Manner to the Egg Extracellular Matrix Is Homologous to von Willebrand FactorPublished by Elsevier BV ,1995
- Nucleotide sequence and peptide motifs of mouse uromodulin (Tamm-Horsfall protein) - the most abundant protein in mammalian urineBiochimica et Biophysica Acta (BBA) - Gene Structure and Expression, 1995
- The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: Causes and consequencesHuman Genetics, 1992
- A large domain common to sperm receptors (Zp2 and Zp3) and TGF‐β type III receptorFEBS Letters, 1992
- A single gene encodes membrane-bound and free forms of GP-2, the major glycoprotein in pancreatic secretory (zymogen) granule membranes.Proceedings of the National Academy of Sciences of the United States of America, 1991
- Amino acid sequence and domain structure of entactin. Homology with epidermal growth factor precursor and low density lipoprotein receptor.The Journal of cell biology, 1988
- Polypeptide composition of the mammalian tectorial membraneHearing Research, 1987
- Uromodulin (Tamm-Horsfall Glycoprotein): a Renal Ligand for LymphokinesScience, 1987