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INF2 mutations in Charcot‐Marie‐Tooth disease complicated with focal segmental glomerulosclerosis
Author(s) -
Toyota Kentaro,
Ogino Daisuke,
Hayashi Makiko,
Taki Masashi,
Saito Kayoko,
Abe Akiko,
Hashimoto Taeko,
Umetsu Kazuo,
Tsukaguchi Hiroyasu,
Hayasaka Kiyoshi
Publication year - 2013
Publication title -
journal of the peripheral nervous system
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1
H-Index - 67
eISSN - 1529-8027
pISSN - 1085-9489
DOI - 10.1111/jns5.12014
Subject(s) - medicine , focal segmental glomerulosclerosis , weakness , muscle biopsy , pes cavus , atrophy , muscle weakness , muscle atrophy , abnormality , proteinuria , pediatrics , pathology , biopsy , surgery , kidney , complication , psychiatry
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