Dietary L-tyrosine supplementation in nemaline myopathy.
about
Congenital myopathies: an updateNemaline body myopathy caused by a novel mutation in troponin T1 (TNNT1)Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1).Consensus statement on standard of care for congenital myopathies.Skeletal muscle α-actin diseases (actinopathies): pathology and mechanisms.Sarcomere Dysfunction in Nemaline Myopathy.Novel autosomal dominant TNNT1 mutation causing nemaline myopathy.Cardiac α-actin over-expression therapy in dominant ACTA1 disease.Treating pediatric neuromuscular disorders: The future is now.Testing of therapies in a novel nebulin nemaline myopathy model demonstrate a lack of efficacy.Hypertrophy and dietary tyrosine ameliorate the phenotypes of a mouse model of severe nemaline myopathy
P2860
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P2860
Dietary L-tyrosine supplementation in nemaline myopathy.
description
2007 nî lūn-bûn
@nan
2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Dietary L-tyrosine supplementation in nemaline myopathy.
@ast
Dietary L-tyrosine supplementation in nemaline myopathy.
@en
Dietary L-tyrosine supplementation in nemaline myopathy.
@nl
type
label
Dietary L-tyrosine supplementation in nemaline myopathy.
@ast
Dietary L-tyrosine supplementation in nemaline myopathy.
@en
Dietary L-tyrosine supplementation in nemaline myopathy.
@nl
prefLabel
Dietary L-tyrosine supplementation in nemaline myopathy.
@ast
Dietary L-tyrosine supplementation in nemaline myopathy.
@en
Dietary L-tyrosine supplementation in nemaline myopathy.
@nl
P2093
P2860
P356
P1476
Dietary L-tyrosine supplementation in nemaline myopathy
@en
P2093
Andrew J Kornberg
Carolyn Ellaway
Catherine Sy
David Ketteridge
Kathryn N North
Laurence G Roddick
Sian Rudge
Susan T Iannaccone
P2860
P304
P356
10.1177/0883073807309794
P50
P577
2007-12-13T00:00:00Z