Associated Papers
Whole exome sequencing reveals a biallelic frameshift mutation in GRXCR2 in hearing impairment in Cameroon.
Wonkam A et al.
Molecular Genetics & Genomic Medicine, 2021
33528103 (PubMed )
Supplement: MGG3-9-e1609-s001.pdf
Whole exome sequencing in three families segregating a pediatric case of sarcoidosis.
Calender A et al.
Bmc Medical Genomics, 2018
29510755 (PubMed )
Supplement: 12920_2018_338_MOESM6_ESM.xlsx › T2
Grxcr2 is required for stereocilia morphogenesis in the cochlea.
Avenarius MR et al.
Plos One, 2018
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