Letter to the Editor
Cockayne syndrome B with axonal sensorimotor polyneuropathy caused by a de novo mutation of the gene ERCC6: A novel phenotypic and genotypic variant
Síndrome de Cockayne B con polineuropatía sensitivomotora axonal causada por una mutación de novo del gen ERCC6: una nueva variante fenotípica y genotípica
a Department of General Medicine, Burdwan Medical College and Hospital, Burdwan, West Bengal, India
b Section of Clinical Neurophysiology, Department of Neurology, University Hospital “La Paz”, Madrid, Spain
c Department of Neuromedicine, Bankura Sammilani Medical College and Hospital, Bankura, West Bengal, India
d Department of Neuromedicine, Bangur Institute of Neurosciences, Kolkata, West Bengal, India
e Department of Neurology, University Hospital “12 de Octubre”, Madrid, Spain
f Research Institute (i+12), University Hospital “12 de Octubre”, Madrid, Spain
g Centro de Investigación Biomédica en Red Sobre Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain
h Department of Medicine, Complutense University, Madrid, Spain
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