Hereditary peripheral neuropathies diagnosed by next-generation sequencing | Tidsskrift for Den norske legeforening
Alanyl-tRNA synthetase mutation in a family with dominant distal hereditary motor neuropathy
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The given table describes the different types of Distal Hereditary... | Download Scientific Diagram
Distal hereditary motor neuropathy in Korean patients with a small heat shock protein 27 mutation | Experimental & Molecular Medicine
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
A family with distal hereditary motor neuropathy and a K141Q mutation of small heat shock protein HSPB1. | Semantic Scholar
Children | Free Full-Text | Differential Diagnosis of Acquired and Hereditary Neuropathies in Children and Adolescents—Consensus-Based Practice Guidelines
Distal hereditary motor neuropathy, type II: MedlinePlus Genetics
Frontiers | Genetic and Clinical Features in 24 Chinese Distal Hereditary Motor Neuropathy Families
Clinical, Genetic, and Disability Profile of Pediatric Distal Hereditary Motor Neuropathy
The distal hereditary motor neuropathies | Journal of Neurology, Neurosurgery & Psychiatry
Further Validation of the SIGMAR1 c.151+1G>T Mutation as Cause of Distal Hereditary Motor Neuropathy | Semantic Scholar
Hereditary Motor and Sensory Neuropathies | Pediatric Annals
Hereditary Motor Syndromes
Frontiers | A Novel Mutation of GARS in a Chinese Family With Distal Hereditary Motor Neuropathy Type V
Distal hereditary motor neuropathy with vocal cord paresis: from difficulty in choral singing to a molecular genetic diagnosis | Practical Neurology
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,
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
distal hereditary motor neuropathy - YouTube
Charcot-Marie-Tooth disease and hereditary motor neuropathies – Update 2020
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
Ayurvedic Concept Of Hereditary Motor Sensory Neuropathy
A SIGMAR1 splice-site mutation causes distal hereditary motor neuropathy | Neurology
Charcot-Marie-Tooth disease and hereditary motor neuropathies – Update 2020
Variants in MME are associated with autosomal‐recessive distal hered
