Pre-Spliceosomal Binding of U1 Small Nuclear Ribonucleoprotein (RNP) and Heterogenous Nuclear RNP E1 Is Associated with Suppression of a Growth Hormone Receptor Pseudoexon
Author:
Affiliation:
1. Department of Endocrinology, St. Bartholomew’s Hospital, London EC1A 7BE, United Kingdom
Publisher
The Endocrine Society
Subject
Endocrinology,Molecular Biology,General Medicine
Link
http://academic.oup.com/mend/article-pdf/21/10/2529/8960050/mend2529.pdf
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3. A rapid screening for steroid 21-hydroxylase mutations in patients with congenital adrenal hyperplasia. Mutations in brief no. 247. Online.;Kapelari;Hum Mutat,1999
4. Germline mutations in the multiple endocrine neoplasia type 1 gene: evidence for frequent splicing defects.;Mutch;Hum Mutat,1999
5. Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1.;Ars;Hum Mol Genet,2000
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