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Article

Physical mapping and genomic structure of the Lowe syndrome gene OCRL1

27 Jan 1997

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9048911
DOI: 10.1007/s004390050329

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Related research

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Physical mapping and genomic structure of the Lowe syndrome gene OCRL1PMID 9048911Read ↗

Novel OCRL1 gene mutations in six Chinese families with Lowe syndrome.Semantic proximity Read ↗

[A case report of genetic analysis in the OCRL1 gene in Lowe syndrome].Semantic proximity Read ↗

Characterization of a germline mosaicism in families with Lowe syndrome, and identification of seven novel mutations in the OCRL1 gene.Semantic proximity Read ↗

OCRL mutation analysis in Italian patients with Lowe syndrome.Semantic proximity Read ↗

Structure and function of the Lowe syndrome protein OCRL1.Semantic proximity Read ↗

Novel mutation of OCRL1 in Lowe syndrome.Semantic proximity Read ↗

Chromosome mapping of the Emr1 gene.Semantic proximity Read ↗

[Analysis of OCRL gene variant in a Chinese pedigree affected with Lowe syndrome].Semantic proximity Read ↗

Novel mutation of OCRL1 in Lowe syndrome with multiple epidermal cysts.Semantic proximity Read ↗

Identification of OCRL1 mutations in two Taiwanese Lowe syndrome patients.Semantic proximity Read ↗

Inositol 5-phosphatases: insights from the Lowe syndrome protein OCRLSemantic proximity Read ↗

Mutations are not uniformly distributed throughout the OCRL1 gene in Lowe syndrome patients.Semantic proximity Read ↗

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