Novel human pathological mutations. Gene symbol: PROS1. Disease: Protein S deficiency

Autor:	Alhenc-Gelas M, Delphine Borgel, Gandrille S, Aa, Garcia, Pintao M, Ph, Reitsma, Ca, Spek, Mc, Visser
Přispěvatelé:	Amsterdam institute for Infection and Immunity, Cancer Center Amsterdam, Center of Experimental and Molecular Medicine
Rok vydání:	2010
Předmět:	Protein S Deficiency Gene Duplication Hormonal regulation [IGMD 6] Humans Blood Proteins Exons Protein S
Zdroj:	Scopus-Elsevier Europe PubMed Central Human Genetics, 127, 1, pp. 121-121 Human genetics, 127(1). Springer Verlag Human Genetics, 127, 121-121
ISSN:	0340-6717
Popis:	Item does not contain fulltext 01 januari 2010
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e09461b0066df97e7fe9486974d968df https://hdl.handle.net/2066/89913 Zobrazit plný text záznamu Full text from SpringerLink