Dystroglycanopathies: Genetic Bases of Muscular Dystrophies Due to Alteration in the O-Glycosylation of α-Dystroglycan-Reference-Cited by-同舟云学术

Dystroglycanopathies: Genetic Bases of Muscular Dystrophies Due to Alteration in the O-Glycosylation of α-Dystroglycan

Published:2023 Issue: Volume:11 Page:
ISSN:2326-4594
Container-title:Journal of Inborn Errors of Metabolism and Screening
language:
Short-container-title:J. inborn errors metab. screen.

Author:

Cubilla M.A.¹,Papazoglu G.M.¹,Asteggiano C.G.²^ORCID

Affiliation:

1. Hospital de Niños de la Santísima Trinidad, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas, Argentina

2. Hospital de Niños de la Santísima Trinidad, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas, Argentina; Universidad Católica de Córdoba, Argentina

Publisher

FapUNIFESP (SciELO)

Subject

Genetics (clinical),Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Link

http://www.scielo.br/scielo.php?script=sci_pdf&pid=S2326-45942023000100301&tlng=en

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2. Congenital muscular dystrophy and congenital myopathy;Butterfield RJ;Contin Lifelong Learn Neurol,2019

3. Differentiating congenital myopathy from congenital muscular dystrophy;Harmelink M;Clin Perinatol,2020

4. Congenital muscular dystrophies: What is new?;Zambon AA;Neuromuscul Disord,2021

5. Congenital muscular dystrophy type 1A with residual merosin expression;Kim HJ;Korean J Pediatr,2014

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1. The congenital muscular dystrophies;Annals of the Child Neurology Society;2023-12-20