leucine and Ichthyosis, Lamellar

leucine has been researched along with Ichthyosis, Lamellar in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Akiyama, M; Suga, Y; Sugiura, K1
Akiyama, M; Arita, K; Chaplin, T; Happle, R; Jacyk, WK; McGrath, JA; Mein, CA; Shimizu, H; van Rensburg, EJ; Wessagowit, V1

Other Studies

2 other study(ies) available for leucine and Ichthyosis, Lamellar

ArticleYear
Very mild lamellar ichthyosis with compound heterozygous TGM1 mutations including the novel missense mutation p.Leu693Phe.
    Journal of dermatological science, 2013, Volume: 72, Issue:2

    Topics: Amino Acid Sequence; Arginine; Base Sequence; DNA Mutational Analysis; Heterozygote; Humans; Ichthyosis, Lamellar; Infant; Infant, Newborn; Infant, Newborn, Diseases; Leucine; Male; Molecular Sequence Data; Mutation; Mutation, Missense; Phenylalanine; Prognosis; Protein Structure, Tertiary; Sequence Homology, Amino Acid; Transglutaminases

2013
The South African "bathing suit ichthyosis" is a form of lamellar ichthyosis caused by a homozygous missense mutation, p.R315L, in transglutaminase 1.
    The Journal of investigative dermatology, 2007, Volume: 127, Issue:2

    Topics: Adolescent; Adult; Arginine; Child; Female; Homozygote; Humans; Ichthyosis, Lamellar; Leucine; Male; Mutation, Missense; South Africa; Transglutaminases

2007