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Badanie genu mitofuzyny 2 u polskich pacjentów z aksonalną postacią choroby Charcot-Marie-Tooth
Creator: Contributor:Kochański, Andrzej (Promotor)
Publisher:Medical Research Center Polish Academy of Sciences
Place of publishing: Date issued/created: Description:s.: 81, fotogr., rys., wykr., 30 cm.
Degree name: Level of degree: Degree discipline : Degree grantor:Instytut Medycyny Doświadczalnej i Klinicznej im. M. Mossakowskiego PAN
Subject and Keywords:Genetical diseases ; Neurodegenerative diseases
Abstract:The aim of this work to study the mitofusin 2 mutations' profile in Polish patients with CMT2 as the most common cause of CMT2 disease.
References:Bibliogr. 89 poz.
Resource type: Detailed Resource Type: Format: Source: Language: Rights: Terms of use:Copyright-protected material. May be used within the limits of statutory user freedoms
Digitizing institution:Mossakowski Medical Research Institute PAS
Original in:Library of the Mossakowski Medical Research Institute PAS
Projects co-financed by:Programme Innovative Economy, 2010-2014, Priority Axis 2. R&D infrastructure
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