Literature DB >> 4829426

Application of a quantitative scoring system in the investigation of some hereditary neurological disorders.

H Skre.   

Abstract

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Year:  1974        PMID： 4829426     DOI： 10.1111/j.1399-0004.1974.tb01678.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  3 in total

1.  MFN2 point mutations occur in 3.4% of Charcot-Marie-Tooth families. An investigation of 232 Norwegian CMT families.

Authors:  Geir J Braathen; Jette C Sand; Ana Lobato; Helle Høyer; Michael B Russell
Journal:  BMC Med Genet       Date:  2010-03-29       Impact factor: 2.103

2.  Two novel connexin32 mutations cause early onset X-linked Charcot-Marie-Tooth disease.

Authors:  Geir J Braathen; Jette C Sand; Geir Bukholm; Michael B Russell
Journal:  BMC Neurol       Date:  2007-07-09       Impact factor: 2.474

3.  Highly diverse flavobacterial phages isolated from North Sea spring blooms.

Authors:  Nina Bartlau; Antje Wichels; Georg Krohne; Evelien M Adriaenssens; Anneke Heins; Bernhard M Fuchs; Rudolf Amann; Cristina Moraru
Journal:  ISME J       Date:  2021-09-02       Impact factor: 10.302
  3 in total

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