Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Deafness and PTPRQ[original query] |
---|
Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing. Molecular genetics & genomic medicine 2015 May 3 (3): 189-96. Ammar-Khodja Fatima, Bonnet Crystel, Dahmani Malika, Ouhab Sofiane, Lefèvre Gaelle M, Ibrahim Hassina, Hardelin Jean-Pierre, Weil Dominique, Louha Malek, Petit Christi |
Identification of Novel PTPRQ and MYO1A Mutations in An Iranian Pedigree with Autosomal Recessive Hearing Loss. Cell journal 2018 1 20 (1): 127-131. Talebi Farah, Ghanbari Mardasi Farideh, Mohammadi Asl Javad, Tizno Saeed, Najafvand Zadeh Marzi |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 29, 2023
- Content source: