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Article

Clinical phenotypes of MAGEL2 mutations and deletions.

Orphanet journal of rare diseases - 25 Mar 2014

Buiting Karin, Di Donato Nataliya, Beygo Jasmin, Bens Susanne, von der Hagen Maja, Hackmann Karl, Horsthemke Bernhard

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Topics

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Share to Child, Preschool
Share to Chromosomes, Human, Pair 15
Share to Gene Deletion
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Promoter Regions, Genetic

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Source

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Identifiers

PMID: 24661356
DOI: 10.1186/1750-1172-9-40
PMCID: PMC3987887

Genes

MAGEL2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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