Literature DB >> 8990016

Novel mutation of the myelin P0 gene in a CMT1B family.

E Sorour1, J MacMillan, M Upadhyaya.   

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Year:  1997        PMID： 8990016     DOI： 10.1002/(SICI)1098-1004(1997)9:1<74::AID-HUMU16>3.0.CO;2-M

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


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  4 in total

1.  Steroid responsive polyneuropathy in a family with a novel myelin protein zero mutation.

Authors:  M Donaghy; S M Sisodiya; R Kennett; B McDonald; N Haites; C Bell
Journal:  J Neurol Neurosurg Psychiatry       Date:  2000-12       Impact factor: 10.154

2.  Genetic spectrum of hereditary neuropathies with onset in the first year of life.

Authors:  Jonathan Baets; Tine Deconinck; Els De Vriendt; Magdalena Zimoń; Laetitia Yperzeele; Kim Van Hoorenbeeck; Kristien Peeters; Ronen Spiegel; Yesim Parman; Berten Ceulemans; Patrick Van Bogaert; Adolf Pou-Serradell; Günther Bernert; Argirios Dinopoulos; Michaela Auer-Grumbach; Satu-Leena Sallinen; Gian Maria Fabrizi; Fernand Pauly; Peter Van den Bergh; Birdal Bilir; Esra Battaloglu; Ricardo E Madrid; Dagmara Kabzińska; Andrzej Kochanski; Haluk Topaloglu; Geoffrey Miller; Albena Jordanova; Vincent Timmerman; Peter De Jonghe
Journal:  Brain       Date:  2011-08-11       Impact factor: 13.501

3.  Genetic and clinical spectrums in Korean Charcot-Marie-Tooth disease patients with myelin protein zero mutations.

Authors:  Hye Jin Kim; Soo Hyun Nam; Hye Mi Kwon; Si On Lim; Jae Hong Park; Hyun Su Kim; Sang Beom Kim; Kyung Suk Lee; Ji Eun Lee; Byung-Ok Choi; Ki Wha Chung
Journal:  Mol Genet Genomic Med       Date:  2021-04-06       Impact factor: 2.183

4.  How Does Protein Zero Assemble Compact Myelin?

Authors:  Arne Raasakka; Petri Kursula
Journal:  Cells       Date:  2020-08-04       Impact factor: 6.600
  4 in total

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