Overview of the classification and genetics of hereditary peripheral neuropathies and rare unclassified forms | SpringerLink
Distal hereditary motor neuropathy type V - Wikipedia
Distal hereditary motor neuropathy in Korean patients with a small heat shock protein 27 mutation | Experimental & Molecular Medicine
Genes | Free Full-Text | Identification of a Novel de Novo Variant in the SYT2 Gene Causing a Rare Type of Distal Hereditary Motor Neuropathy
Approach to Inherited Neuropathies - ppt video online download
Charcot-Marie-Tooth Neuropathy with Pyramidal Features | SpringerLink
Genetic classification of distal hereditary motor neuropathies | Download Table
The distal hereditary motor neuropathies | Journal of Neurology, Neurosurgery & Psychiatry
The given table describes the different types of Distal Hereditary... | Download Scientific Diagram
A family with distal hereditary motor neuropathy and a K141Q mutation of small heat shock protein HSPB1. | Semantic Scholar
Hereditary Motor Syndromes
Alanyl-tRNA synthetase mutation in a family with dominant distal hereditary motor neuropathy
Amazon.com: Reversing Distal Hereditary Motor Neuropathy: Deficiencies The Raw Vegan Plant-Based Detoxification & Regeneration Workbook for Healing Patients. Volume 4: 9781395362492: Central, Health: Libros
Hereditary sensory motor polyneuropathy - Gabbasova - Pediatric Traumatology, Orthopaedics and Reconstructive Surgery
Distal hereditary motor neuropathy, type V: MedlinePlus Genetics
A knock-in/knock-out mouse model of HSPB8-associated distal hereditary motor neuropathy and myopathy reveals toxic gain-of-function of mutant Hspb8
Variants in MME are associated with autosomal‐recessive distal hered
Hereditary Neuropathy Foundation - Could you be 1 of the estimated 3300 patients in the US with the gene causing SORD Deficiency? You may have been diagnosed with CMT2, or distal hereditary
Hereditary Motor and Sensory Neuropathies | Pediatric Annals
Brain on X: "Jacquier et al. describe a new homozygous variant in the COQ7 gene in a family with distal hereditary motor neuropathy. They show that the variant affects coenzyme Q10 production,
Variable phenotypic expression and onset in MYH14 distal hereditary motor neuropathy phenotype in a large, multigenerational North American family. - Abstract - Europe PMC
PDF) Distal Hereditary Motor Neuropathy Type II (Distal HMN Type II): Phenotype and Molecular Genetics | Vincent Timmerman - Academia.edu
The role of genetic mutations in genes HSPB1 & HSPB8 in Distal Hereditary Motor Neuropathy, type II Syndrome | Auctores
Figure 2 from A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy | Semantic Scholar
Hereditary peripheral neuropathies diagnosed by next-generation sequencing | Tidsskrift for Den norske legeforening
Pathomechanisms of genes reported in hereditary motor neuropathy (HMN) | Download Scientific Diagram
