[Experience in molecular diagnostic in hereditary neuropathies in a pediatric tertiary hospital]. [electronic resource]
Producer: 20160920Description: 490-8 p. digitalISSN:- 1576-6578
- Adolescent
- Cell Cycle Proteins -- genetics
- Charcot-Marie-Tooth Disease -- classification
- Child
- Child, Preschool
- Connexins -- genetics
- Consanguinity
- Demyelinating Diseases -- diagnosis
- Female
- GTP Phosphohydrolases -- genetics
- Hereditary Sensory and Motor Neuropathy -- diagnosis
- Hospitals, Pediatric -- statistics & numerical data
- Humans
- Intracellular Signaling Peptides and Proteins -- genetics
- Male
- Mitochondrial Proteins -- genetics
- Molecular Diagnostic Techniques
- Myelin Proteins -- genetics
- Nerve Tissue Proteins -- genetics
- Retrospective Studies
- Roma -- genetics
- Spain -- epidemiology
- TRPV Cation Channels -- genetics
- Tertiary Care Centers -- statistics & numerical data
- Gap Junction beta-1 Protein
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Publication Type: English Abstract; Journal Article
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