Pages that link to "Q36581402"
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The following pages link to Integrating population variation and protein structural analysis to improve clinical interpretation of missense variation: application to the WD40 domain (Q36581402):
Displaying 9 items.
- Structure of the MeCP2-TBLR1 complex reveals a molecular basis for Rett syndrome and related disorders (Q33594773) (← links)
- WD40 repeat domain proteins: a novel target class? (Q47291150) (← links)
- Recon3D enables a three-dimensional view of gene variation in human metabolism. (Q49850956) (← links)
- Accurate prediction of functional, structural, and stability changes in PITX2 mutations using in silico bioinformatics algorithms. (Q54981073) (← links)
- On the verge of diagnosis: Detection, reporting, and investigation of de novo variants in novel genes identified by clinical sequencing (Q57455560) (← links)
- A NGS-Targeted Autism/ID Panel Reveals Compound Heterozygous GNB5 Variants in a Novel Patient (Q60958172) (← links)
- Nuclear receptor corepressors in intellectual disability and autism (Q89602927) (← links)
- Histone Deacetylase 3 Governs Perinatal Cerebral Development via Neural Stem and Progenitor Cells (Q90379378) (← links)
- Computing the Pathogenicity of Alzheimer's Disease Presenilin 1 Mutations (Q91220593) (← links)