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

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

Research

Studies (1)

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

Authors

Authors	Studies
Hayasaka, K; Ikeda, H; Ikegami, T; Ishida, A; Johnston, H; Nicholson, G; Ouvrier, R; Wise, G	1

Other Studies

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

Article	Year
De novo mutation of the myelin Po gene in Déjérine-Sottas disease (hereditary motor and sensory neuropathy type III): two amino acid insertion after Asp 118. Human mutation, 1998, Volume: Suppl 1 Topics: Alleles; Amino Acid Sequence; Base Sequence; DNA; DNA Mutational Analysis; Family Health; Fatal Outcome; Female; Hereditary Sensory and Motor Neuropathy; Humans; Infant; Male; Mutagenesis, Insertional; Mutation; Myelin P0 Protein; Pedigree; Phenylalanine; Polymerase Chain Reaction; Tyrosine	1998

Article

Year

De novo mutation of the myelin Po gene in Déjérine-Sottas disease (hereditary motor and sensory neuropathy type III): two amino acid insertion after Asp 118.

Human mutation, 1998, Volume: Suppl 1

Topics: Alleles; Amino Acid Sequence; Base Sequence; DNA; DNA Mutational Analysis; Family Health; Fatal Outcome; Female; Hereditary Sensory and Motor Neuropathy; Humans; Infant; Male; Mutagenesis, Insertional; Mutation; Myelin P0 Protein; Pedigree; Phenylalanine; Polymerase Chain Reaction; Tyrosine

1998