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Publications by N. Kiely
Deletion of P2 Promoter of GJB1 Gene a Cause of Charcot-Marie-Tooth Disease
Neuromuscular Disorders
Child Health
Neurology
Pediatrics
Perinatology
Genetics
Familial Russell–Silver Syndrome Like Phenotype in the PCNA Domain of the CDKN1C Gene, a Further Case
Case Reports in Genetics
Related publications
Charcot–Marie–Tooth Disease
MORC2mutations Cause Axonal Charcot-Marie-Tooth Disease With Pyramidal Signs
Annals of Neurology
Neurology
Charcot-Marie-Tooth Disease Type 2R
A Novel GJB1 Mutation Associated With X‐linked Charcot–Marie–Tooth Disease in a Large Chinese Family Pedigree
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Charcot-Marie-Tooth Disease. A Practical Guide
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Update on Charcot-Marie-Tooth Disease
Current Neurology and Neuroscience Reports
Neuroscience
Neurology
Charcot-Marie-Tooth Disease Type 2B5
Charcot-Marie-Tooth Disease Type 4G
Diagnosis and Care of Charcot-Marie-Tooth Disease
Clinical Neurology
Neurology
