Linda Peters

Linda Peters

University of Waikato - Hamilton / New Zealand
Medical and Health Sciences / Medical Genetics
AD Scientific Index ID: 125997
person_outline Linda Peters's MOST POPULAR ARTICLES
1-) Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23 The American Journal of Human Genetics 68 (1), 26-37, 2001
2-) Chitosan: A review of sources and preparation methods International Journal of Biological Macromolecules 169, 85-94, 2021
3-) Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function Nature genetics 30 (3), 277-284, 2002
4-) Chitosan: A review of molecular structure, bioactivities and interactions with the human body and micro-organisms Carbohydrate Polymers 282, 119132, 2022
5-) Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28 Human molecular genetics 11 (23), 2877-2885, 2002