The given table describes the different types of Distal Hereditary... | Download Scientific Diagram
Distal hereditary motor neuropathy with vocal cord paresis: from difficulty in choral singing to a molecular genetic diagnosis | Practical Neurology
Charcot-Marie-Tooth Neuropathy with Pyramidal Features | SpringerLink
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Hereditary Motor Syndromes
Alanyl-tRNA synthetase mutation in a family with dominant distal hereditary motor neuropathy
Hereditary neuropathies | PPT
Altered TDP‐43‐dependent splicing in HSPB8‐related distal hereditary motor neuropathy and myofibrillar myopathy - Cortese - 2018 - European Journal of Neurology - Wiley Online Library
X-Linked Distal Hereditary Motor Neuropathy disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
The genetics of Charcot–Marie–Tooth disease: current trend | TACG
Distal Hereditary Motor Neuropathy Type 7 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
The distal hereditary motor neuropathies | Journal of Neurology, Neurosurgery & Psychiatry
Charcot-Marie-Tooth disease and hereditary motor neuropathies – Update 2020
A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID | Journal of Human Genetics
Variable phenotypic expression and onset in MYH14 distal hereditary motor neuropathy phenotype in a large, multigenerational North American family. - Abstract - Europe PMC
Hereditary motor and sensory neuropathy | PPT
A knock-in/knock-out mouse model of HSPB8-associated distal hereditary motor neuropathy and myopathy reveals toxic gain-of-function of mutant Hspb8
Hereditary peripheral neuropathies diagnosed by next-generation sequencing | Tidsskrift for Den norske legeforening
Reversing Distal Hereditary Motor Neuropathy: Success Stories Part 1 The Raw Vegan Plant-Based Detoxification & Regeneration Workbook for Healing Patients. Volume 6 : Amazon.sg: Books
Distal hereditary motor neuropathy, type II: MedlinePlus Genetics
Frontiers | A Novel Mutation of GARS in a Chinese Family With Distal Hereditary Motor Neuropathy Type V
Further Validation of the SIGMAR1 c.151+1G>T Mutation as Cause of Distal Hereditary Motor Neuropathy | Semantic Scholar
Figure 2 from A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy | Semantic Scholar
Clinical, Genetic, and Disability Profile of Pediatric Distal Hereditary Motor Neuropathy | Neurology
