leucine and Autosomal Dominant Myotubular Myopathy

leucine has been researched along with Autosomal Dominant Myotubular Myopathy in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (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
Bitoun, M; Bönnemann, C; Buj-Bello, A; Guicheney, P; Jungbluth, H; Muntoni, F; Robb, S; Sewry, CA; Treves, S; Zhou, H	1

Other Studies

2 other study(ies) available for leucine 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
Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene. Neuromuscular disorders : NMD, 2007, Volume: 17, Issue:4 Topics: Adolescent; Calcium; Cresols; DNA Mutational Analysis; Dose-Response Relationship, Drug; Female; Genes, Dominant; Humans; Leucine; Magnetic Resonance Imaging; Muscle, Skeletal; Mutation, Missense; Myopathies, Structural, Congenital; Potassium Chloride; Ryanodine Receptor Calcium Release Channel; Serine	2007

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

Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene.

Neuromuscular disorders : NMD, 2007, Volume: 17, Issue:4

Topics: Adolescent; Calcium; Cresols; DNA Mutational Analysis; Dose-Response Relationship, Drug; Female; Genes, Dominant; Humans; Leucine; Magnetic Resonance Imaging; Muscle, Skeletal; Mutation, Missense; Myopathies, Structural, Congenital; Potassium Chloride; Ryanodine Receptor Calcium Release Channel; Serine

2007