valine and Klein Syndrome

valine has been researched along with Klein Syndrome 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
Cremers, CW; Geurds, MP; Hamel, BC; Hol, FA; Mariman, EC	1

Other Studies

1 other study(ies) available for valine and Klein Syndrome

Article	Year
Identification of two PAX3 mutations causing Waardenburg syndrome, one within the paired domain (M62V) and the other downstream of the homeodomain (Q282X). Human mutation, 1998, Volume: Suppl 1 Topics: Amino Acid Sequence; Amino Acid Substitution; Base Sequence; Binding Sites; Codon, Terminator; DNA; DNA Mutational Analysis; DNA-Binding Proteins; Family Health; Fatal Outcome; Female; Glutamine; Humans; Infant, Newborn; Methionine; Mutation; Paired Box Transcription Factors; PAX3 Transcription Factor; Point Mutation; Polymorphism, Single-Stranded Conformational; Transcription Factors; Valine; Waardenburg Syndrome	1998

Article

Year

Identification of two PAX3 mutations causing Waardenburg syndrome, one within the paired domain (M62V) and the other downstream of the homeodomain (Q282X).

Human mutation, 1998, Volume: Suppl 1

Topics: Amino Acid Sequence; Amino Acid Substitution; Base Sequence; Binding Sites; Codon, Terminator; DNA; DNA Mutational Analysis; DNA-Binding Proteins; Family Health; Fatal Outcome; Female; Glutamine; Humans; Infant, Newborn; Methionine; Mutation; Paired Box Transcription Factors; PAX3 Transcription Factor; Point Mutation; Polymorphism, Single-Stranded Conformational; Transcription Factors; Valine; Waardenburg Syndrome

1998