Intrafamilial variability in GMPPB-associated dystroglycanopathy: Broadening of the phenotype-Reference-Cited by-同舟云学术

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Intrafamilial variability in GMPPB-associated dystroglycanopathy: Broadening of the phenotype

Published:2015-03-13 Issue:14 Volume:84 Page:1495-1497
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Bharucha-Goebel D. X.,Neil E.,Donkervoort S.,Dastgir J.,Wiggs E.,Winder T. L.,Moore S. A.,Iannaccone S. T.,Bonnemann C. G.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. MRI for the diagnosis of limb girdle muscular dystrophies;Current Opinion in Neurology;2024-08-12

2. Early onset LGMDR19 with unusual features related to GMPPB gene in South Indian siblings with variable phenotype;Neurology Asia;2024-06

3. GDP-Mannose Pyrophosphorylase B (GMPPB)-Related Disorders;Genes;2023-01-31

4. Epidemiology of congenital disorders of glycosylation (CDG)—overview and perspectives;Journal of Rare Diseases;2022-12-07

5. Clinico‐genetic spectrum of limb‐girdle muscular weakness in Austria: A multicentre cohort study;European Journal of Neurology;2022-03-10

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