Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases.
about
Form and function: the laminin family of heterotrimersThe expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and reviewMerosin and congenital muscular dystrophyImmunocytochemical analysis of human muscular dystrophy.Differential protein expression and basal lamina remodeling in human heart failureMolecular basis of muscular dystrophies.Laminins of the neuromuscular system.Laminins and human disease.Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42.The extracellular matrix of muscle--implications for manipulation of the craniofacial musculature.Diagnostic immunohistology of muscle diseases.Laminin polymerization induces a receptor-cytoskeleton networkCongenital muscular dystrophy. Part I: a review of phenotypical and diagnostic aspects.Laminin α2 Deficiency-Related Muscular Dystrophy Mimicking Emery-Dreifuss and Collagen VI related DiseasesRegulation of the blood-testis barrier by a local axis in the testis: role of laminin α2 in the basement membrane.Congenital muscular dystrophy in Arab children.Domain IV of mouse laminin beta1 and beta2 chains.Identification of Two Novel LAMA2 Mutations in a Chinese Patient with Congenital Muscular Dystrophy.Genotype/phenotype analysis in Chinese laminin-α2 deficient congenital muscular dystrophy patients
P2860
Q22254277-D9063998-4BB9-4C82-8A04-8902503D2491Q24680748-104B6BF9-8744-49F0-B110-27B9844C792AQ28145060-02752E71-0DF1-4A5A-95B5-D7D7DB089F60Q33840931-7A724724-EA74-4E31-821F-65045900F912Q33925177-5821670D-6F21-40C1-9222-F7A6826BAB83Q34044147-270EA975-43D5-4C17-9937-AB16FBA02A99Q34071971-7AB7F8A6-EC86-46DC-8D8F-87C259CA3394Q34071975-3E96BA1B-E549-406C-8999-8D13FF3C5D1CQ34145035-7338E508-35C5-4831-8009-01E541C92F0BQ34352280-805E0B36-7084-49FB-8336-7DBE6089B331Q36085905-CF0E9141-F72E-4BCF-934C-FD456588E4E6Q36342173-AD6ECD37-4B02-4E00-B1D9-D6B136306F48Q37426320-EAA4248F-B2F7-4E60-8DB2-E952938E07F5Q37589611-D10F2F8B-9B96-4BC4-A874-DA5190CFA0EBQ42501409-EFBB209D-B4CD-48C9-B7F3-38FDC185E117Q45226643-6E9E5DBD-FB13-49E2-9E40-B1DA1016657CQ45713806-5FCEEDD8-8E7F-4F46-9AE7-61182C5744A8Q50326365-E430B35F-5A55-40FB-85EB-0A51492B206EQ57317698-C4EFF96B-D5F2-4E5C-9AC6-1844EE8C2646
P2860
Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
1998年學術文章
@zh
1998年學術文章
@zh-hant
name
Laminin alpha2 chain-deficient ...... sion in severe and mild cases.
@en
Laminin alpha2 chain-deficient ...... sion in severe and mild cases.
@nl
type
label
Laminin alpha2 chain-deficient ...... sion in severe and mild cases.
@en
Laminin alpha2 chain-deficient ...... sion in severe and mild cases.
@nl
prefLabel
Laminin alpha2 chain-deficient ...... sion in severe and mild cases.
@en
Laminin alpha2 chain-deficient ...... sion in severe and mild cases.
@nl
P2093
P356
P1433
P1476
Laminin alpha2 chain-deficient ...... sion in severe and mild cases.
@en
P2093
P304
P356
10.1212/WNL.51.1.94
P407
P577
1998-07-01T00:00:00Z