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KCTD7
Identi Cation of Novel Biomarkers for Metabolic Syndrome Based On
Novel Mutations Consolidate KCTD7 As a Progressive Myoclonus Epilepsy Gene
The KCTD Family of Proteins: Structure, Function, Disease Relevance Zhepeng Liu1†, Yaqian Xiang2† and Guihong Sun1*
Genome-Wide Joint SNP and CNV Analysis of Aortic Root Diameter in African Americans: the Hypergen Study Nathan E
Genomic Rearrangements of the 7Q11-21 Region
UNIVERSITY of CALIFORNIA Los Angeles Identification of a Multisubunit E3 Ubiquitin Ligase Required for Heterotrimeric G-Protein
Identification of New Risk Factors for Rolandic Epilepsy: CNV at Xp22.31
Constitutional SAMD9L Mutations Cause Familial Myelodysplastic Syndrome and Transient Monosomy 7
The CLN3 Gene and Protein: What We Know
Dissection of the Genetic Background of Childhood Onset Progressive Myoclonic Epilepsies
Structure and Function of Multimeric BTB Proteins and Cullin3 Substrate Adaptors
An Unusual Clinical Severity of 16P11.2 Deletion Syndrome Caused by Unmasked Recessive Mutation of CLN3
Exome Sequencing Identifies Compound Heterozygous KCTD7
KCTD: a New Gene Family Involved in Neurodevelopmental and Neuropsychiatric Disorders
KCTD7-Related Progressive Myoclonus Epilepsy
KCTD7 Deficiency Defines a Distinct Neurodegenerative Disorder with a Conserved Autophagy-Lysosome Defect Kyle A
Progressive Myoclonic Epilepsy-Associated Gene Kctd7 Regulates Retinal Neurovascular Patterning and Function T
Identification of Rare-Disease Genes Using Blood Transcriptome Sequencing and Large Control Cohorts
Top View
You Can Check If Genes Are Captured by the Agilent Sureselect V5 Exome
Genetic Characteristics of Non-Familial Epilepsy
Copy Number Networks to Guide Combinatorial Therapy for Cancer and Other Disorders
Identification of Rare-Disease Genes in Diverse Undiagnosed Cases Using
“Atypical” Phenotypes of Neuronal Ceroid Lipofuscinosis
Therapeutic Landscape for Batten Disease: Current Treatments and Future Prospects
Study Title Here
Genes with High Penetrance for Syndromic and Non-Syndromic Autism Typically Function Within the Nucleus and Regulate Gene Expression Emily L
The Clinical and Molecular Consequences of Mutations in Epilepsy Gene KCTD7
Clinician-Centric Diagnosis of Rare Genetic Diseases: Performance of a Gene Pertinence Metric in Decision Support for Clinicians Michael M
Genes with High Penetrance for Syndromic and Non-Syndromic Autism Typically Function Within the Nucleus and Regulate Gene Expression Emily L
Emerging New Roles of the Lysosome and Neuronal Ceroid Lipofuscinoses Anil B
Supplementary Table 1. a Full List of Cancer Genes