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An Indian child with lipoid proteinosis resulting from a recurrent frameshift mutation (507delT) in the extracellular matrix protein 1 gene
Author(s) -
Chan I.,
Bingewar G.,
Patil K.,
Nayak C.,
Wadhwa S.L.,
McGrath J.A.
Publication year - 2004
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/j.1365-2133.2004.06159.x
Subject(s) - frameshift mutation , medicine , dermatology , family medicine , mutation , genetics , gene , biology

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