UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

A novel clinical phenotype of myopathy, sensorimotor neuropathy, infertility, and hypogonadism with multiple mitochondrial DNA deletions

Quigley, A; Reardon, K; Kapsa, R; Dennett, X; Byrne, E; Thyagarajan, D; (2001) A novel clinical phenotype of myopathy, sensorimotor neuropathy, infertility, and hypogonadism with multiple mitochondrial DNA deletions. Journal of Clinical Neuromuscular Disease , 3 (2) 77 - 82.

Full text not available from this repository.


Type:Article
Title:A novel clinical phenotype of myopathy, sensorimotor neuropathy, infertility, and hypogonadism with multiple mitochondrial DNA deletions
Keywords:myopathy, sensorimotor neuropathy
UCL classification:UCL > School of Life and Medical Sciences > Faculty of Medical Sciences

Archive Staff Only: edit this record