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Identification, phenotype correlation and functional analysis of novel mutations in Arylsulfatase E in patients with X-linked recessive brachytelephalangic chondrodysplasia punctata phenotype

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Identiferoai:union.ndltd.org:mcgill.ca/oai:escholarship.mcgill.ca:s1784q59d
Date January 2011
CreatorsMatos-Miranda, Claudia
ContributorsNancy Braverman (Supervisor)
PublisherMcGill University
Source SetsMcGill University
Languagehttp://id.loc.gov/vocabulary/iso639-2/eng
Detected LanguageEnglish
TypeThesis
RightsAll items in eScholarship@McGill are protected by copyright with all rights reserved unless otherwise indicated.
RelationPid: 103762

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