Associated Papers
A 127 kb truncating deletion of PGRMC1 is a novel cause of X-linked isolated paediatric cataract.
Jones JL et al.
European Journal of Human Genetics : Ejhg, 2021
Exome and genome sequencing of nasopharynx cancer identifies NF-κB pathway activating mutations.
Li YY et al.
Nature Communications, 2017
28098136 (PubMed )
Supplement: ncomms14121-s5.xlsx › WES_NPC_MAF__N_111_
A novel locus for X-linked congenital cataract on Xq24.
Craig JE et al.
Molecular Vision, 2008
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