Associated Papers
Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy.
Takata A et al.
Nature Communications, 2019
31175295 (PubMed )
Supplement: 41467_2019_10482_MOESM8_ESM.xlsx › Supplementary_Data_5
Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family.
Okutman O et al.
Human Molecular Genetics, 2015
Six polymorphisms in genes involved in DNA double-strand break repair and chromosome synapsis: association with male infertility.
Zhang X et al.
Systems Biology in Reproductive Medicine, 2015
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