Compounds > proline

proline and Charcot-Marie-Tooth Disease, Demyelinating, Type 4f

proline has been researched along with Charcot-Marie-Tooth Disease, Demyelinating, Type 4f in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Mechler, F; Molnar, MJ; Siska, E; Szabo, A; Züchner, S1
Ekici, AB; Grehl, H; Korinthenberg, R; Park, O; Rautenstrauss, B1

Other Studies

2 other study(ies) available for proline and Charcot-Marie-Tooth Disease, Demyelinating, Type 4f

ArticleYear
Marked phenotypic variation in a family with a new myelin protein zero mutation.
    Neuromuscular disorders : NMD, 2005, Volume: 15, Issue:11

    Topics: Adult; DNA Mutational Analysis; Family Health; Female; Hereditary Sensory and Motor Neuropathy; Humans; Leucine; Male; Mutation; Myelin P0 Protein; Neural Conduction; Pedigree; Phenotype; Proline

2005
T>C transition in codon 72 (TCG-->CCG), S72P, a putative hotspot in PMP22.
    Human mutation, 2001, Volume: 17, Issue:1

    Topics: Amino Acid Substitution; Codon; Cytosine; Hereditary Sensory and Motor Neuropathy; Humans; Mutation, Missense; Myelin Proteins; Proline; Serine; Thymine

2001