Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases

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Standard

Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases. / Cohn, R D; Herrmann, R; Sorokin, L; Wewer, U M; Voit, T.

I: Neurology, Bind 51, Nr. 1, 01.07.1998, s. 94-100.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Cohn, RD, Herrmann, R, Sorokin, L, Wewer, UM & Voit, T 1998, 'Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases', Neurology, bind 51, nr. 1, s. 94-100.

APA

Cohn, R. D., Herrmann, R., Sorokin, L., Wewer, U. M., & Voit, T. (1998). Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases. Neurology, 51(1), 94-100.

Vancouver

Cohn RD, Herrmann R, Sorokin L, Wewer UM, Voit T. Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases. Neurology. 1998 jul. 1;51(1):94-100.

Author

Cohn, R D ; Herrmann, R ; Sorokin, L ; Wewer, U M ; Voit, T. / Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases. I: Neurology. 1998 ; Bind 51, Nr. 1. s. 94-100.

Bibtex

@article{855bf6e5f5924d1c80878f35f12093fd,
title = "Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases",
abstract = "To characterize the expression of distinct fragments of laminin alpha2 chain in patients with partial laminin alpha2 chain deficiency and variable clinical severity.",
keywords = "Adult, Antibodies, Basement Membrane, Child, Preschool, Epitopes, Fluorescent Antibody Technique, Gene Expression, Humans, Infant, Infant, Newborn, Laminin, Muscular Dystrophies, Phenotype, Protein Structure, Tertiary",
author = "Cohn, {R D} and R Herrmann and L Sorokin and Wewer, {U M} and T Voit",
year = "1998",
month = jul,
day = "1",
language = "English",
volume = "51",
pages = "94--100",
journal = "Neurology",
issn = "0028-3878",
publisher = "Lippincott Williams & Wilkins",
number = "1",

}

RIS

TY - JOUR

T1 - Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases

AU - Cohn, R D

AU - Herrmann, R

AU - Sorokin, L

AU - Wewer, U M

AU - Voit, T

PY - 1998/7/1

Y1 - 1998/7/1

N2 - To characterize the expression of distinct fragments of laminin alpha2 chain in patients with partial laminin alpha2 chain deficiency and variable clinical severity.

AB - To characterize the expression of distinct fragments of laminin alpha2 chain in patients with partial laminin alpha2 chain deficiency and variable clinical severity.

KW - Adult

KW - Antibodies

KW - Basement Membrane

KW - Child, Preschool

KW - Epitopes

KW - Fluorescent Antibody Technique

KW - Gene Expression

KW - Humans

KW - Infant

KW - Infant, Newborn

KW - Laminin

KW - Muscular Dystrophies

KW - Phenotype

KW - Protein Structure, Tertiary

M3 - Journal article

C2 - 9674785

VL - 51

SP - 94

EP - 100

JO - Neurology

JF - Neurology

SN - 0028-3878

IS - 1

ER -

ID: 34325844