A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21.
about
A human skeletal muscle interactome centered on proteins involved in muscular dystrophies: LGMD interactomeLimb-girdle muscular dystrophies: where next after six decades from the first proposal (Review).RNAi-based gene therapy for dominant Limb Girdle Muscular Dystrophies.A novel autosomal dominant inclusion body myopathy linked to 7q22.1-31.1.A new locus on 3p23-p25 for an autosomal-dominant limb-girdle muscular dystrophy, LGMD1HExome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy.Neuromuscular disorders: genes, genetic counseling and therapeutic trialsThe Classification, Natural History and Treatment of the Limb Girdle Muscular DystrophiesTargeted mRNA Decay by RNA Binding Protein AUF1 Regulates Adult Muscle Stem Cell Fate, Promoting Skeletal Muscle Integrity.Genetic basis of limb-girdle muscular dystrophies: the 2014 updateThe Growing Family of Limb-Girdle Muscular Dystrophies: Old and Newly Identified Members.Clinical phenotype, muscle MRI and muscle pathology of LGMD1F.Further defining the critical genes for the 4q21 microdeletion disorder.A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G).Hutterite brothers both affected with two forms of limb girdle muscular dystrophy: LGMD2H and LGMD2I
P2860
Q24317313-5D03538A-7452-4D93-874D-C48D6950FBEAQ33608787-0FB3A0B8-5FD6-4CE7-9278-39498E9654EFQ33996884-31DA1536-5021-44DA-BC9F-CA908A46A436Q34314374-D85D7768-D3D8-4068-A14D-D53E6CD68EB0Q34329134-7CC11A1D-34D7-497E-B8FD-1674DF0DCD33Q35857041-751068AA-CCCF-4503-B48D-150963BA99E6Q37217303-48032CD2-5C6E-41CE-9450-F57B6D001543Q37610524-99732E8A-EF31-4CDB-8A17-B85CE60CA8F7Q37662074-0DB1D588-FBD0-4BA5-857D-0D71A3B6B81CQ38213016-81B58DD8-66F5-42B3-A476-C2B96E18FBCFQ38528085-B609F7BE-616C-4717-BA5E-9C1941A85E19Q45916393-15DC2E3B-2EFD-45AD-B700-93303B6D1C4EQ52122106-D6630628-471E-4CC5-9F84-797310ED8243Q53061543-4AF17027-A868-4384-A136-FF2BC8F7F6D3Q58856656-132ECCB7-D50A-4E94-B677-DD84016E6822
P2860
A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh-hant
name
A new form of autosomal domina ...... ation maps to chromosome 4p21.
@en
A new form of autosomal dominant limb-girdle muscular dystrophy
@nl
type
label
A new form of autosomal domina ...... ation maps to chromosome 4p21.
@en
A new form of autosomal dominant limb-girdle muscular dystrophy
@nl
prefLabel
A new form of autosomal domina ...... ation maps to chromosome 4p21.
@en
A new form of autosomal dominant limb-girdle muscular dystrophy
@nl
P2860
P50
P356
P1476
A new form of autosomal domina ...... ation maps to chromosome 4p21.
@en
P2093
Alessandra Starling
Fernando Kok
P2860
P2888
P304
P356
10.1038/SJ.EJHG.5201289
P577
2004-12-01T00:00:00Z
P5875
P6179
1012704106