Phenotypic expression of late-onset glycogen storage disease type II: identification of asymptomatic adults through family studies and review of reported families-Reference-Cited by-同舟云学术

Phenotypic expression of late-onset glycogen storage disease type II: identification of asymptomatic adults through family studies and review of reported families

Published:2000-10 Issue:7 Volume:10 Page:467-471
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Ausems Margreet G.E.M,ten Berg Klara,Beemer Frits A,Wokke John H.J

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference29 articles.

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4. Respiratory failure as initial symptom of acid maltase deficiency;Keunen;J Neurol Neurosurg Psychiat,1984

5. Genotype–phenotype correlation in adult-onset acid maltase deficiency;Wokke;Ann Neurol,1995

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