Clinical features and genetic findings in patients with Charcot Marie Tooth Disease Type 2 (CMT2) due to LRSAM1 mutation

Authors :: Andrea Cortese
Julian Blake
Matilde Laura
Alexander M. Rossor
James M. Polke
H Houlden
Mary M. Reilly
M.P. Lunn
R. Poh
Pedro J. Tomaselli
Source :: Neuromuscular Disorders. 27:S25
Publication Year :: 2017
Publisher :: Elsevier BV, 2017.

Subjects :: Tooth disease
Neurology
business.industry
Pediatrics, Perinatology and Child Health
Mutation (genetic algorithm)
Physiology
Medicine
In patient
Neurology (clinical)
business
Bioinformatics
Genetics (clinical)
Clinical neurology

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