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SBF2
Inherited Neuropathies
Redefining the Specificity of Phosphoinositide-Binding by Human
Molecular and Genetic Medicine
Inherited Neuropathies: Emerging Genetic Therapies
Nº Ref Uniprot Proteína Péptidos Identificados Por MS/MS 1 P01024
An Epigenome-Wide Association Study Based on Cell Type
Variation in Protein Coding Genes Identifies Information Flow
Biophysical Characterization of the Human K0513 Protein
Related Protein-13/Set-Binding Factor-2
Gnomad Lof Supplement
The Role of the Myotubularin Pseudophosphatase MTMR13 In
SBF1 Mutations Associated with Autosomal Recessive Axonal Neuropathy with Cranial Nerve Involvement
Mouse Sbf2 Knockout Project (CRISPR/Cas9)
Redefining the Specificity of Phosphoinositide-Binding By
Genetic Heterogeneity of Asthma Pheno- Types Identified by a Clustering Approach
Charcot-Marie-Tooth 4B2 Caused by a Novel Mutation in the MTMR13/SBF2 Gene in Two Related Portuguese Families
Blueprint Genetics Charcot-Marie-Tooth Neuropathy
Charcot-Marie-Tooth Gene, SBF2, Associated with Taxane- Induced Peripheral Neuropathy in African Americans
Top View
Felipe Fidalgo De Carvalho
Downloaded from ENCODE and Aligned to the Human Genome (Grch38 Release 95) Using Hisat2 (V2.1.0)
The 2020 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun
Identification of a Novel SBF2 Frameshift Mutation in Charcot
Clinical and Electrophysiological Aspects of Charcot-Marie-Tooth Disease
Overlapping Molecular Pathological Themes Link Charcot–Marie–Tooth Neuropathies and Hereditary Spastic Paraplegias
Investigation of the Function of Myotubularin Through
The Phosphoinositide 3-Phosphatase MTMR2 Interacts with PSD-95 and Maintains Excitatory Synapses by Modulating Endosomal Traffic
(MTMR)2 Phosphatidylinositol Phosphatase by MTMR5, a Catalytically Inactive Phosphatase
Molecular Mechanisms of Inherited Demyelinating Neuropathies
Splicing Mutation in Sbf1 Causes Nonsyndromic Male Infertility in the Rat
Emerging Roles of a Pivotal Lncrna SBF2-AS1 in Cancers