valine and Autosomal Dominant Myotubular Myopathy

valine has been researched along with Autosomal Dominant Myotubular Myopathy 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	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Clarke, NF; Dye, DE; Hagiwara, T; Kobayashi, Y; Laing, NG; Liyanage, K; Nishino, I; Nonaka, I; North, KN; Ouvrier, R; Shimakawa, S; Sparrow, JC; Walker, KR	1

Other Studies

1 other study(ies) available for valine and Autosomal Dominant Myotubular Myopathy

Article	Year
Actin mutations are one cause of congenital fibre type disproportion. Annals of neurology, 2004, Volume: 56, Issue:5 Topics: Actins; Adenosine Triphosphatases; Aspartic Acid; Biopsy; Child, Preschool; DNA Mutational Analysis; Female; Heterozygote; Humans; Infant; Infant, Newborn; Leucine; Male; Models, Molecular; Muscle Fibers, Slow-Twitch; Muscle, Skeletal; Mutation, Missense; Myopathies, Structural, Congenital; Proline; Sequence Analysis, Protein; Serine; Valine	2004

Article

Year

Actin mutations are one cause of congenital fibre type disproportion.

Annals of neurology, 2004, Volume: 56, Issue:5

Topics: Actins; Adenosine Triphosphatases; Aspartic Acid; Biopsy; Child, Preschool; DNA Mutational Analysis; Female; Heterozygote; Humans; Infant; Infant, Newborn; Leucine; Male; Models, Molecular; Muscle Fibers, Slow-Twitch; Muscle, Skeletal; Mutation, Missense; Myopathies, Structural, Congenital; Proline; Sequence Analysis, Protein; Serine; Valine

2004