about
A novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth diseaseA novel c.5308_5311delGAGA mutation in Senataxin in a Cypriot family with an autosomal recessive cerebellar ataxia.Down-regulation of myogenin can reverse terminal muscle cell differentiationGenomic and genetic studies of systemic sclerosis: A systematic review.A novel PMP22 mutation Ser22Phe in a family with hereditary neuropathy with liability to pressure palsies and CMT1A phenotypes.P-8. Molecular genetic studies of Charcot-Marie-Tooth disease in the Cypriot population.Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X.Genetic findings of Cypriot spinal muscular atrophy patients.Twist induces reversal of myotube formation.Charcot-Marie-Tooth Disease in Cyprus: Epidemiological, Clinical and Genetic CharacteristicsA novel GDAP1 mutation 439delA is associated with autosomal recessive CMT disease
P50
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P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Paschalis Nicolaou
@ast
Paschalis Nicolaou
@en
Paschalis Nicolaou
@es
Paschalis Nicolaou
@nl
type
label
Paschalis Nicolaou
@ast
Paschalis Nicolaou
@en
Paschalis Nicolaou
@es
Paschalis Nicolaou
@nl
prefLabel
Paschalis Nicolaou
@ast
Paschalis Nicolaou
@en
Paschalis Nicolaou
@es
Paschalis Nicolaou
@nl
P106
P31
P496
0000-0002-1425-2917