L239F founder mutation in GDAPI is associated with a mild Charcot-Marie-Tooth type 4C4 (CMT4C4) phenotype

Bibliographische Detailangaben

Veröffentlicht in:	Neurogenetics 2010, Vol.11 (3), p.357-366
Hauptverfasser:	KABZINSKA, Dagmara, STRUGALSKA-CYNOWSKA, Halina, TIMMERMAN, Vincent, GUERGUELTCHEVA, Velina, TOURNEV, Ivailo, SARAFOV, Stayko, DE JONGHE, Peter, JORDANOVA, Albena, HAUSMANOWA-PETRUSEWICZ, Irena, KOCHANSKI, Andrzej, KOSTERA-PRUSZCZYK, Anna, RYNIEWICZ, Barbara, POSMYK, Renata, MIDRO, Alina, SEEMAN, Pavel, BARANKOVA, Lucia, ZIMON, Magdalena, BAETS, Jonathan
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Fundamental and applied biological sciences. Psychology Genetics of eukaryotes. Biological and molecular evolution Human Medical sciences Molecular and cellular biology Neurology Population genetics, reproduction patterns Vertebrates: nervous system and sense organs
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