Associated Papers
Further evidence from DNAH12 supports favorable fertility outcomes of infertile males with dynein axonemal heavy chain gene family variants.
Geng H et al.
Iscience, 2024
39071892 (PubMed )
Supplement: mmc2.xlsx › Sheet1
Whole-genome sequencing identifies rare missense variants of WNT16 and ERVW-1 causing the systemic lupus erythematosus.
Chen J et al.
Genomics, 2022
The role of genetics in neurodegenerative dementia: a large cohort study in South China.
Jiao B et al.
Npj Genomic Medicine, 2021
34389718 (PubMed )
Supplement: 41525_2021_235_MOESM1_ESM.docx
Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts.
Vesa J et al.
Neuromuscular Disorders : Nmd, 2009
CADASIL in Arabs: clinical and genetic findings.
Bohlega S et al.
Bmc Medical Genetics, 2007
Mutational analysis of human BAFF receptor TNFRSF13C (BAFF-R) in patients with common variable immunodeficiency.
Losi CG et al.
Journal of Clinical Immunology, 2005
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