Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Biochemistry and molecular genetics of human glycogenoses: an overview.

Muscle & nerve. Supplement - 1 Jan 1995

DiMauro S, Tsujino S, Shanske S, Rowland L P

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Base Sequence
Share to Brain Diseases
Share to Glycogen Debranching Enzyme System
Share to Glycogen Storage Disease

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Heart Diseases

Share to Muscular Diseases

Share to Neuromuscular Diseases

Share to Phosphorylases

Source

Identifiers

PMID: 7603508
DOI: 10.1002/mus.880181405

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Biochemistry and molecular genetics of human glycogenoses: an overview.PMID 7603508Read ↗

Molecular Genetics of Type 1 Glycogen Storage DiseasesSemantic proximity Read ↗

Glycogen Storage Diseases: A Brief Review and Update on Clinical Features, Genetic Abnormalities, Pathologic Features, and TreatmentSemantic proximity Read ↗

Glycogen storage disease type I: Genetic etiology, clinical manifestations, and conventional and gene therapiesSemantic proximity Read ↗

Glycogen pathways in disease: new developments in a classical field of medical geneticsSemantic proximity Read ↗

Diagnosis and management of glycogen storage diseases type VI and IX: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)Semantic proximity Read ↗

[Hepatic glycogen storage diseases: Symptoms, management and associated mutations].Semantic proximity Read ↗

Glycogen storage disease Ia complicated with multiple hepatic adenomas: a case report and literature reviewSemantic proximity Read ↗

[Glycogen branching enzyme deficiency (Andersen disease)].Semantic proximity Read ↗

Update on new muscle glycogenosis.Semantic proximity Read ↗

Glycogen storage disease type I: diagnosis and phenotype/genotype correlationSemantic proximity Read ↗

Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex.Semantic proximity Read ↗

Evaluation of Glycogen Storage Patients: Report of Twelve Novel Variants and New Clinical Findings in a Turkish Population.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.