Literature DB >> 9452099

Mutation analysis in Charcot-Marie-Tooth disease type 1 (CMT1).

E Sorour1, M Upadhyaya.   

Abstract

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Year:  1998        PMID： 9452099     DOI： 10.1002/humu.1380110178

Source DB:  PubMed          Journal:  Hum Mutat        ISSN： 1059-7794            Impact factor:   4.878


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  2 in total

1.  Dysmyelinating and demyelinating Charcot-Marie-Tooth disease associated with two myelin protein zero gene mutations.

Authors:  Hanna Drac; Dagmara Kabzińska; Izabela Moszyńska; Halina Strugalska-Cynowska; Irena Hausmanowa-Petrusewicz; Andrzej Kochański
Journal:  J Appl Genet       Date:  2010-11-03       Impact factor: 3.240

2.  Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene.

Authors:  Oranee Sanmaneechai; Shawna Feely; Steven S Scherer; David N Herrmann; Joshua Burns; Francesco Muntoni; Jun Li; Carly E Siskind; John W Day; Matilde Laura; Charlotte J Sumner; Thomas E Lloyd; Sindhu Ramchandren; Rosemary R Shy; Tiffany Grider; Chelsea Bacon; Richard S Finkel; Sabrina W Yum; Isabella Moroni; Giuseppe Piscosquito; Davide Pareyson; Mary M Reilly; Michael E Shy
Journal:  Brain       Date:  2015-08-25       Impact factor: 13.501
  2 in total

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