Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.
about
Galectin-1 Protein Therapy Prevents Pathology and Improves Muscle Function in the mdx Mouse Model of Duchenne Muscular DystrophyA new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2.Predicted and observed sizes of dystrophin in some patients with gene deletions that disrupt the open reading frame.Analysis of RFLPs and DNA deletions in the Chinese Duchenne muscular dystrophy geneScreening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencingSkeletal muscle homeostasis in duchenne muscular dystrophy: modulating autophagy as a promising therapeutic strategy.A comprehensive database of Duchenne and Becker muscular dystrophy patients (0-18 years old) in East ChinaDuplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotypegenotype correlationCharacteristics of Japanese Duchenne and Becker muscular dystrophy patients in a novel Japanese national registry of muscular dystrophy (Remudy).Modulation of Protein Quality Control and Proteasome to Autophagy Switch in Immortalized Myoblasts from Duchenne Muscular Dystrophy Patients.Targeting muscle stem cell intrinsic defects to treat Duchenne muscular dystrophy.Characteristics of Japanese Patients with Becker Muscular Dystrophy and Intermediate Muscular Dystrophy in a Japanese National Registry of Muscular Dystrophy (Remudy): Heterogeneity and Clinical Variation.
P2860
Q27318308-62617255-D34D-452D-A206-018A253945FEQ30502688-3DC38884-A01B-4826-B6F4-1EFA127C2BF6Q33594782-98F3A7EA-8022-45EF-A188-CE4ADB47ECA3Q33596646-0A3406AB-C9A8-4E0E-AEC4-F15386167C71Q33597405-EF14D0F8-FA24-44AF-8C60-21B1D990F7A2Q33843901-F67B4969-C6CE-4193-856E-B04158712606Q33944130-C2F7E2D6-8782-4FF9-A9CB-DB70E10471C8Q34459245-E05444A2-77A8-4DF3-AD33-403E4147E900Q35198016-47161A53-8B63-4C5C-8193-7851AD6758E1Q36803129-AE466802-D90E-4D48-86CD-3B3A42726F09Q47216956-0F6485F3-5E22-4954-9F56-8D9CC7265A85Q55063443-2D6C1C01-FCAF-429C-A1E7-8B982C736D14Q55475347-F60D8492-74BB-4147-9DED-8EF38D2FA1CF
P2860
Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.
description
1988 nî lūn-bûn
@nan
1988 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Mild and severe muscular dystr ...... p21 of the human X chromosome.
@ast
Mild and severe muscular dystr ...... p21 of the human X chromosome.
@en
type
label
Mild and severe muscular dystr ...... p21 of the human X chromosome.
@ast
Mild and severe muscular dystr ...... p21 of the human X chromosome.
@en
prefLabel
Mild and severe muscular dystr ...... p21 of the human X chromosome.
@ast
Mild and severe muscular dystr ...... p21 of the human X chromosome.
@en
P2093
P2860
P1476
Mild and severe muscular dystr ...... p21 of the human X chromosome.
@en
P2093
K E Davies
P2860
P407
P577
1988-01-01T00:00:00Z