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Published byEmanuele Leoni Modified over 5 years ago
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Multiple Endocrine Neoplasia Type 2B and Hirschsprung’s Disease
Raj P. Kapur Clinical Gastroenterology and Hepatology Volume 3, Issue 5, Pages (May 2005) DOI: /S (04) Copyright © 2005 American Gastroenterological Association Terms and Conditions
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Figure 1 Location and nature of RET mutations associated with MEN2A, MEN2B, and FMTC (A), as well as a subset of reported mutations associated with HSCR (B). SP, signal peptide; grey ovals, cysteine residues affected in MEN2A or FMTC; TK, tyrosine kinase domain; X, substituted amino acid; -, stop codon. Adapted from Chakravarti,17 Eng and Mulligan,4 and Yip et al.3 Clinical Gastroenterology and Hepatology 2005 3, DOI: ( /S (04) ) Copyright © 2005 American Gastroenterological Association Terms and Conditions
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