Associated Papers
Indicators of HSV1 Infection, ECM-Receptor Interaction, and Chromatin Modulation in a Nuclear Family with Schizophrenia.
Huang YC et al.
Journal of Personalized Medicine, 2023
37763159 (PubMed )
Supplement: jpm-13-01392-s001.zip › Supplementary_Table_S3.xlsx › Variants
Mutation update of SERPING1 related to hereditary angioedema in the Chinese population.
Wang X et al.
Hereditas, 2022
FINCA syndrome-Defining neurobehavioral phenotype in survivors into late childhood.
Badura-Stronka M et al.
Molecular Genetics & Genomic Medicine, 2022
35255187 (PubMed )
Supplement: MGG3-10-e1899-s002.xlsx › P11
Hereditary angioedema in a Jordanian family with a novel missense mutation in the C1-inhibitor N-terminal domain.
Jaradat SA et al.
Molecular Immunology, 2016
Two novel mutations of FBN1 in Jordanian patients with Marfan syndrome.
Jaradat SA et al.
International Journal of Clinical and Experimental Medicine, 2015
Select a paper to view details