Lack of hormone binding in COS-7 cells expressing a mutated growth hormone receptor found in Laron dwarfism.

A single point mutation in the growth hormone (GH) receptor gene generating a Phe-->Ser substitution in the extracellular binding domain of the receptor has been identified in one family with Laron type dwarfism. The mutation was introduced by site-directed mutagenesis into cDNAs encoding the ful...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Edery, M, Rozakis-Adcock, M, Goujon, L, Finidori, J, Lévi-Meyrueis, C, Paly, J, Djiane, J, Postel-Vinay, M C, Kelly, P A
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1993
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC288035/
https://ncbi.nlm.nih.gov/pubmed/8450064
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