phenylalanine and Collodion Baby Syndrome

phenylalanine has been researched along with Collodion Baby Syndrome in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Akiyama, M; Suga, Y; Sugiura, K	1

Other Studies

1 other study(ies) available for phenylalanine and Collodion Baby Syndrome

Article	Year
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

Article

Year

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