Associated Papers
Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits.
Yuan B et al.
Genome Medicine, 2022
36180924 (PubMed )
Supplement: 13073_2022_1113_MOESM1_ESM.xlsx › Table_S6
Navigating Hereditary Hearing Loss: Pathology of the Inner Ear.
Nicolson T
Frontiers in Cellular Neuroscience, 2021
Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss.
Li C et al.
Proceedings of the National Academy of Sciences of the United States of America, 2019
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