Severe growth deficiency is associated with STAT5b mutations that disrupt protein folding and activity.

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Bibliographic Details
Title: Severe growth deficiency is associated with STAT5b mutations that disrupt protein folding and activity.
Authors: Varco-Merth B; Department of Biochemistry and Molecular Biology, Oregon Health & Science University, Portland, Oregon 97239-3098, USA., Feigerlová E, Shinde U, Rosenfeld RG, Hwa V, Rotwein P
Source: Molecular endocrinology (Baltimore, Md.) [Mol Endocrinol] 2013 Jan; Vol. 27 (1), pp. 150-61. Date of Electronic Publication: 2012 Nov 16.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
Journal Info: Publisher: Endocrine Society Country of Publication: United States NLM ID: 8801431 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1944-9917 (Electronic) Linking ISSN: 08888809 NLM ISO Abbreviation: Mol Endocrinol Subsets: MEDLINE
Database: MEDLINE Ultimate
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