Null Leukemia Inhibitory Factor Receptor (LIFR) Mutations in Stüve-Wiedemann/Schwartz-Jampel Type 2 Syndrome-Reference-Cited by-同舟云学术

Null Leukemia Inhibitory Factor Receptor (LIFR) Mutations in Stüve-Wiedemann/Schwartz-Jampel Type 2 Syndrome

Published:2004-02 Issue:2 Volume:74 Page:298-305
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Dagoneau Nathalie,Scheffer Deborah,Huber Céline,Al-Gazali Lihadh I.,Di Rocco Maja,Godard Anne,Martinovic Jelena,Raas-Rothschild Annick,Sigaudy Sabine,Unger Sheila,Nicole Sophie,Fontaine Bertrand,Taupin Jean-Luc,Moreau Jean-François,Superti-Furga Andrea,Le Merrer Martine,Bonaventure Jacky,Munnich Arnold,Legeai-Mallet Laurence,Cormier-Daire Valérie

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference26 articles.

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3. Osteoblasts display receptors for and responses to leukemia-inhibitory factor;Allan;J Cell Physiol,1990

4. Mutations in the immunoglobulin-like domain of gp190, the leukemia inhibitory factor (LIF) receptor, increase or decrease its affinity for LIF;Bitard;J Biol Chem,2003

5. Stüve-Wiedemann syndrome and defects of the respiratory chain;Chabrol;Am J Med Genet,1997

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