Erratum: Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses (Journal of Human Genetics (2014) 59 (163-172) DOI: 10.1038/jhg.2013.139));Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses

Journal of Human Genetics

Volumn 59, Issue 3, 2014, Pages 163-172

  Ishiura, Hiroyuki ^a   Takahashi, Yuji ^a   Hayashi, Toshihiro ^a   Saito, Kayoko ^b   Furuya, Hirokazu ^c   Watanabe, Mitsunori ^d   Murata, Miho ^e   Suzuki, Mikiya ^f   Sugiura, Akira ^g   Sawai, Setsu ^h,i   Shibuya, Kazumoto ^h   Ueda, Naohisa ^j,k   Ichikawa, Yaeko ^a   Kanazawa, Ichiro ^l   Goto, Jun ^a   Tsuji, Shoji ^a  

^a UNIVERSITY OF TOKYO   (Japan)

^b TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

^c Omuta National Hospital   (Japan)

^d HIROSAKI UNIVERSITY   (Japan)

^e NATIONAL INSTITUTE OF MENTAL HEALTH   (Japan)

^f Higashisaitama National Hospital   (Japan)

^g SHIZUOKA INSTITUTE OF EPILEPSY AND NEUROLOGICAL DISORDERS   (Japan)

^h CHIBA UNIVERSITY   (Japan)

ⁱ CHIBA UNIVERSITY HOSPITAL   (Japan)

^j Chigasaki Municipal Hospital   (Japan)

^k YOKOHAMA CITY UNIVERSITY   (Japan)

^l INTERNATIONAL UNIVERSITY OF HEALTH AND WELFARE   (Japan)

more..

Author keywords

[No Author keywords available]

Indexed keywords

SPASTIN;

ADOLESCENT; ADULT; AGED; ARTICLE; ATL1 GENE; AUTOSOMAL DOMINANT INHERITANCE; BSCL2 GENE; CHILD; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; CYP7B1 GENE; FEMALE; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; HEREDITARY MOTOR SENSORY NEUROPATHY; HSPD1 GENE; HUMAN; INFANT; JAPANESE; KIAA0196 GENE; KIF5A GENE; L1CAM GENE; MAJOR CLINICAL STUDY; MALE; MICROARRAY ANALYSIS; MIDDLE AGED; MOLECULAR DIAGNOSIS; MOLECULAR EPIDEMIOLOGY; MUTATIONAL ANALYSIS; NEWBORN; NIPA1 GENE; NUCLEOTIDE SEQUENCE; PLP1 GENE; PRESCHOOL CHILD; REEP1 GENE; SCHOOL CHILD; SPAST GENE; SPG11 GENE; SPG20 GENE; SPG21 GENE; SPG7 GENE; YOUNG ADULT; ZFYVE27 GENE; ASIAN CONTINENTAL ANCESTRY GROUP; DEMOGRAPHY; DNA MICROARRAY; FAMILY; GENE DELETION; GENETICS; JAPAN; MOLECULAR GENETICS; MUTATION; SPASTIC PARAPLEGIA, HEREDITARY;

ADOLESCENT; ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; COMPARATIVE GENOMIC HYBRIDIZATION; DEMOGRAPHY; DNA MUTATIONAL ANALYSIS; FAMILY; FEMALE; HUMANS; JAPAN; MALE; MIDDLE AGED; MOLECULAR EPIDEMIOLOGY; MOLECULAR SEQUENCE DATA; MUTATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; SEQUENCE DELETION; SPASTIC PARAPLEGIA, HEREDITARY; YOUNG ADULT;

EID: 84896952872     PISSN: 14345161     EISSN: 1435232X     Source Type: Journal    
DOI: 10.1038/jhg.2015.159     Document Type: Erratum

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