G.P.12.07 A new ACTA1 mutation in two unrelated sporadic cases of neonatal form of CFTD

Autor:	Joël Lunardi, Paulette Mezin, N. Deconinck, Nicole Monnier, Alex Michotte, Mc Commare
Rok vydání:	2009
Předmět:	Genetics Neurology Pediatrics Perinatology and Child Health Mutation (genetic algorithm) Neurology (clinical) Biology Genetics (clinical)
Zdroj:	Neuromuscular Disorders. 19:637
ISSN:	0960-8966
DOI:	10.1016/j.nmd.2009.06.291
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::544daa422c4547255544421e1dc19321 https://doi.org/10.1016/j.nmd.2009.06.291 Zobrazit plný text záznamu Full Text from ScienceDirect