TY  - GEN
AU  - Schraders,Margit
AU  - Oostrik,Jaap
AU  - Huygen,Patrick L M
AU  - Strom,Tim M
AU  - van Wijk,Erwin
AU  - Kunst,Henricus P M
AU  - Hoefsloot,Lies H
AU  - Cremers,Cor W R J
AU  - Admiraal,Ronald J C
AU  - Kremer,Hannie
TI  - Mutations in PTPRQ are a cause of autosomal-recessive nonsyndromic hearing impairment DFNB84 and associated with vestibular dysfunction
SN  - 1537-6605
PY  - 2010///0422
KW  - 5' Untranslated Regions
KW  - genetics
KW  - Amino Acid Sequence
KW  - Case-Control Studies
KW  - Codon, Nonsense
KW  - Cohort Studies
KW  - Female
KW  - Genes, Recessive
KW  - Hearing Loss
KW  - Homozygote
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Molecular Sequence Data
KW  - Pedigree
KW  - Polymorphism, Single Nucleotide
KW  - Receptor-Like Protein Tyrosine Phosphatases, Class 3
KW  - Sequence Homology, Amino Acid
KW  - Vestibular Diseases
KW  - Vestibular Function Tests
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.ajhg.2010.02.015
ER  -