Locations of crossover breakpoints within the CMT1A-REP repeat in Japanese patients with CMT1A and HNPP

Human Genetics

Volumn 99, Issue 2, 1997, Pages 151-154

  Yamamoto, Masahiko ^a   Yasuda, Takeshi ^a   Hayasaka, Kiyoshi ^b   Ohnishi, Akio ^c   Yoshikawa, Hiroo ^d   Yanagihara, Takehiko ^d   Ikegami, Tohru ^b   Yamamoto, Tatsunori ^c   Ohashi, Hirofumi ^e   Nishimura, Tomoya ^d   Mitsuma, Terunori ^f   Kiyosawa, Hidenori ^g   Chance, Phillip F ^g   Sobue, Gen ^a  

^a NAGOYA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b YAMAGATA UNIVERSITY   (Japan)

^c UNIVERSITY OF OCCUPATIONAL AND ENVIRONMENTAL HEALTH   (Japan)

^d OSAKA UNIVERSITY MEDICAL SCHOOL   (Japan)

^e SAITAMA CHILDREN'S MEDICAL CENTER   (Japan)

^f AICHI MEDICAL UNIVERSITY   (Japan)

^g CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 17P; CONTROLLED STUDY; GENE LOCATION; GENE MAPPING; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; JAPAN; MAJOR CLINICAL STUDY; NEUROPATHY; PRIORITY JOURNAL;

ASIAN CONTINENTAL ANCESTRY GROUP; CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOME BREAKAGE; CROSSING OVER, GENETIC; EUROPEAN CONTINENTAL ANCESTRY GROUP; HUMANS; JAPAN; PERIPHERAL NERVOUS SYSTEM DISEASES; REPETITIVE SEQUENCES, NUCLEIC ACID;

EID: 17144461625     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050330     Document Type: Article

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