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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 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
Detailed Clinical Features of PTPRQ-Associated Hearing Loss Identified in a Large Japanese Hearing Loss Cohort.
Genes 2024 4 15 (4): .
Naoko Sakuma, Shin-Ya Nishio, Shin-Ichi Goto, Yohei Honkura, Kiyoshi Oda, Hidehiko Takeda, Marina Kobayashi, Kozo Kumakawa, Satoshi Iwasaki, Masahiro Takahashi, Taku Ito, Yasuhiro Arai, Yasuhiro Isono, Natsuko Obara, Takeshi Matsunobu, Kimihiro Okubo, Shin-Ichi Usa
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