asparagine and Chondrodystrophic Myotonia

asparagine has been researched along with Chondrodystrophic Myotonia in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Aftimos, S; Kannu, P	1
Ezquieta Zubicaray, B; González Gancedo, P; Gracia Bouthelier, R; Iguacel, AO; Jariego Fente, CM; Varela Junquera, JM	1

Other Studies

2 other study(ies) available for asparagine and Chondrodystrophic Myotonia

Article	Year
FGFR3 mutations and medial temporal lobe dysgenesis. Journal of child neurology, 2007, Volume: 22, Issue:2 Topics: Asparagine; Child, Preschool; Humans; Lysine; Magnetic Resonance Imaging; Male; Mutation; Osteochondrodysplasias; Receptor, Fibroblast Growth Factor, Type 3; Temporal Lobe	2007
[Gly380Arg and Asn540Lys mutations of fibroblast growth factor receptor 3 in achondroplasia and hypochndroplasia in the Spanish population]. Medicina clinica, 1999, Mar-06, Volume: 112, Issue:8 Topics: Achondroplasia; Arginine; Asparagine; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 4; Genetic Counseling; Glycine; Humans; Lysine; Osteochondrodysplasias; Phenotype; Point Mutation; Protein-Tyrosine Kinases; Receptors, Fibroblast Growth Factor; RNA, Transfer, Amino Acid-Specific; Spain	1999

Article

Year

FGFR3 mutations and medial temporal lobe dysgenesis.

Journal of child neurology, 2007, Volume: 22, Issue:2

Topics: Asparagine; Child, Preschool; Humans; Lysine; Magnetic Resonance Imaging; Male; Mutation; Osteochondrodysplasias; Receptor, Fibroblast Growth Factor, Type 3; Temporal Lobe

2007

[Gly380Arg and Asn540Lys mutations of fibroblast growth factor receptor 3 in achondroplasia and hypochndroplasia in the Spanish population].

Medicina clinica, 1999, Mar-06, Volume: 112, Issue:8

Topics: Achondroplasia; Arginine; Asparagine; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 4; Genetic Counseling; Glycine; Humans; Lysine; Osteochondrodysplasias; Phenotype; Point Mutation; Protein-Tyrosine Kinases; Receptors, Fibroblast Growth Factor; RNA, Transfer, Amino Acid-Specific; Spain

1999