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Article

Analysis of three mutations in Turkish children with Gaucher disease.

Journal of inherited metabolic disease - 1 Dec 1999

Gürakan F, Terzioğlu M, Koçak N, Yüce A, Ozen H, Ciliv G, Emre S

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

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Source

Identifiers

PMID: 10604154
DOI: 10.1023/a:1005668230365

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.

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

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Analysis of three mutations in Turkish children with Gaucher disease.PMID 10604154Read ↗

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Identification of novel mutations in glucocerebrosidase (GBA) gene in Indian patients with gaucher disease (GD)Semantic proximity Read ↗

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Identification of a new mutation (P178S) in an African-American patient with type 2 Gaucher disease.Semantic proximity Read ↗

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Mutational analysis in a patient with a variant form of Gaucher disease caused by SAP-2 deficiencySemantic proximity Read ↗

Molecular analysis of Turkish Gaucher disease patients: identification of novel mutations in glucocerebrosidase (GBA) gene.Semantic proximity Read ↗

Analysis of the β-glucocerebrosidase gene in Turkish Gaucher disease patients: mutation profile and description of a novel mutant allele.Semantic proximity Read ↗

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