Research article summary (published 30 Jul 2006):

New compound heterozygous mutations in a Chinese family with lipoid proteinosis.

Full Abstract

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Author information

Author/s: Wang, C Y (CY); Zhang, P Z (PZ); Zhang, F R (FR); Liu, J (J); Tian, H Q (HQ); Yu, L (L);

Affiliation: Shandong Provincial Institute of Dermatology and Venereology, 57 Jiyan Road, Jinan, China.

Journal and publication information

Publication Type: Case Reports; Journal Article

Journal: The British journal of dermatology (Br J Dermatol), published in England. (Language: eng)

Reference: 2006-Aug; vol 155 (issue 2) : pp 470-2

Dates: Created 2006/08/02; Completed 2006/11/30;

PMID: 16882193, status: MEDLINE (last retrieval date: 12/26/2008)

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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MeSH headings (categories)

This article was linked to the MESH Headings shown below.

Adult Base Sequence Codon, Nonsense Extracellular Matrix Proteins - genetics Female Heterozygote

Heterozygote Humans Lipoid Proteinosis of Urbach and Wiethe - genetics; pathology Male Molecular Sequence Data Mutation, Missense

Associated Chemicals: Codon, Nonsense (0) ; ECM1 protein, human (0) ; Extracellular Matrix Proteins (0)

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