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ALG13
Congenital Disorders of Glycosylation from a Neurological Perspective
De Novo Mutations in Epileptic Encephalopathies
Associated with Low Dehydrodolichol Diphosphate Synthase (DHDDS) Activity S
Supplementary Table S1. List of Differentially Expressed
Characterization of X-Linked SNP Genotypic Variation in Globally Distributed Human Populations Genome Biology 2010, 11:R10
Targeted Next-Generation Sequencing in Patients with Suggestive X-Linked Intellectual Disability
Alg13/Alg14 UDP-Glcnac Transferase
Landscape of X Chromosome Inactivation Across Human Tissues Taru Tukiainen1,2, Alexandra-Chloé Villani2,3, Angela Yen2,4, Manuel A
Predominant and Novel De Novo Variants in 29 Individuals with ALG13 Deficiency: Clinical
The Phenotypic Spectrum of X‐Linked, Infantile Onset ALG13‐Related
The Transcriptomic Architecture of Mouse Sertoli Cell Clone Embryos Reveals Temporal–Spatial-Specific Reprogramming
Genetic Characteristics of Non-Familial Epilepsy
1 Supplementary Material Figure S1. Volcano Plot of Differentially
The Multiple Evolutionary Origins of the Eukaryotic N-Glycosylation Pathway Jonathan Lombard1,2
Mouse Alg13 Conditional Knockout Project (CRISPR/Cas9)
HHS Public Access Author Manuscript
Description of Strs in Trinucleotide-Repeat Diseases
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