Human Genome Epidemiology Literature Finder
Rare Diseases
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Query Trace: Hereditary Motor And Sensory Neuropathy Type 5[original query] |
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[Spectrum and frequency of mutations in the connexin 32 gene (GJB1) in hereditary and sensory neuropathy type 1X patients from Bashkortostan]. Genetika 2008 Oct 44 (10): 1385-91. Khidiianova I M, Bagautdinova E G, Galieva D V, Krupina N B, Shchagina O A, Tiburkova T B, Magzhanov R V, Poliakov A V, Khusnutdinova E |
Spectrum and frequencies of mutations in the MFN2 gene and its phenotypical expression in Czech hereditary motor and sensory neuropathy type II patients. Molecular medicine reports 2013 Dec 8 (6): 1779-84. Brožková Dana Šafka, Posádka Jan, Laššuthová Petra, Mazanec Radim, Haberlová Jana, Sišková Dana, Sakmaryová Iva, Neupauerová Jana, Seeman Pav |
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