X-linked Charcot-Marie-Tooth Disease
X-linked Charcot-Marie-Tooth Disease
About the Disease
Charcot-Marie-Tooth Disease, X-Linked Dominant, 1, also known as charcot-marie-tooth disease x-linked dominant 1, is related to charcot-marie-tooth disease, x-linked recessive, 2 and charcot-marie-tooth disease, x-linked recessive, 5, and has symptoms including numbness, tremor and paraparesis. An important gene associated with Charcot-Marie-Tooth Disease, X-Linked Dominant, 1 is GJB1 (Gap Junction Protein Beta 1), and among its related pathways/superpathways are Neural crest differentiation and tRNA Aminoacylation. Affiliated tissues include smooth muscle, spinal cord and brain, and related phenotypes are areflexia and sensory neuropathy
Common Targets
G2706 | G5376 | G2705
The "Target / Biomarker Review Report" is a comprehensive and customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about the Target(s) / Biomarker(s) of your choice related to X-linked Charcot-Marie-Tooth Disease, including but not limited to:
• general information;
• protein structure and compound binding;
• protein biological mechanisms;
• its importance;
• the target screening and validation;
• expression level;
• disease relevance;
• drug resistance;
• related combination drugs;
• pharmacochemistry experiments;
• related patent analysis;
• advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai
Other Diseases
X-linked Creatine Transporter Deficiency | X-linked Myotubular Myopathy | X-linked Sideroblastic Anemia | Xeroderma Pigmentosum | Xeroderma Pigmentosum Variant Type | Yellow Fever | Zellweger Syndrome | Zimmermann-Laband Syndrome | Zollinger-Ellison Syndrome | Zygomycosis
