Page last updated: 2024-10-17

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

cytosine has been researched along with Charcot-Marie-Tooth Disease, Demyelinating, Type 4f in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ekici, AB1
Park, O1
Korinthenberg, R1
Grehl, H1
Rautenstrauss, B1

Other Studies

1 other study available for cytosine and Charcot-Marie-Tooth Disease, Demyelinating, Type 4f

ArticleYear
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,

2001