Literature DB >> 3665261

[Clinical and pathological studies on intellectual impairment in Duchenne muscular dystrophy, with special reference to patients with severe intellectual impairment].

T Bandoh, H Kawai, K Adachi, K Ii.   

Abstract

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Year:  1987        PMID： 3665261

Source DB:  PubMed          Journal:  Rinsho Shinkeigaku        ISSN： 0009-918X


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  1 in total

1.  The Xq22 inversion breakpoint interrupted a novel Ras-like GTPase gene in a patient with Duchenne muscular dystrophy and profound mental retardation.

Authors:  Fumiko Saito-Ohara; Yoji Fukuda; Masahiro Ito; Kishan Lal Agarwala; Masaharu Hayashi; Masafumi Matsuo; Issei Imoto; Kazuhiro Yamakawa; Yusuke Nakamura; Johji Inazawa
Journal:  Am J Hum Genet       Date:  2002-07-23       Impact factor: 11.025
  1 in total

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