Open AccessAn Exon Splice Enhancer Mutation Causes Autosomal Dominant GH Deficiency
Author(s) -
C. T. Moseley
Publication year - 2002
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.87.2.847
Subject(s) - ighd , exon , splice site mutation , splice , rna splicing , biology , genetics , enhancer , microbiology and biotechnology , mutation , exon skipping , alternative splicing , intron , exonic splicing enhancer , gene , gene expression , rna , endocrinology , growth hormone , hormone , growth hormone deficiency
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