文献
J-GLOBAL ID:202002285770175008
整理番号:20A0130275
南アジア人集団における創始者変異はインドにおけるFancl Fanconi貧血症例の高有病率をもたらす【JST・京大機械翻訳】
A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India
著者 (24件):
Donovan Frank X.
(Cancer Genomics Unit, Cancer Genetics and Comparative Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland)
,
Solanki Avani
(Department of Cytogenetics, National Institute of Immunohaematology (ICMR), Mumbai, Maharashtra, India)
,
Mori Minako
(Laboratory of DNA Damage Signaling, Department of Late Effects Studies, Radiation Biology Centre, Graduate School of Biostudies, Kyoto University, Kyoto, Japan)
,
Mori Minako
(Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan)
,
Chavan Niranjan
(Department of Cytogenetics, National Institute of Immunohaematology (ICMR), Mumbai, Maharashtra, India)
,
George Merin
(Department of Cytogenetics, National Institute of Immunohaematology (ICMR), Mumbai, Maharashtra, India)
,
C Selvaa Kumar
(School of Biotechnology and Bioinformatics, Level 6, D.Y. Patil Deemed to be University, Navi Mumbai, Maharashtra, India)
,
Okuno Yusuke
(Center for Advanced Medicine and Clinical Research, Nagoya University Hospital, Nagoya, Japan)
,
Muramastsu Hideki
(Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan)
,
Yoshida Kenichi
(Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan)
,
Shimamoto Akira
(Department of Regenerative Medicine Research, Faculty of Pharmaceutical Sciences, Sanyo-Onoda City University, Sanyo Onoda, Yamaguchi, Japan)
,
Takaori-Kondo Akifumi
(Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan)
,
Yabe Hiromasa
(Department of Innovative Medical Science, Tokai University School of Medicine, Isehara, Kanagawa, Japan)
,
Ogawa Seishi
(Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan)
,
Kojima Seiji
(Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan)
,
Yabe Miharu
(Department of Innovative Medical Science, Tokai University School of Medicine, Isehara, Kanagawa, Japan)
,
Ramanagoudr-Bhojappa Ramanagouda
(Cancer Genomics Unit, Cancer Genetics and Comparative Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland)
,
Smogorzewska Agata
(Laboratory of Genome Maintenance, The Rockefeller University, New York, New York)
,
Mohan Sheila
(Apollo Specialty Hospital, Chennai, India)
,
Rajendran Aruna
(Department of Pediatric Hematology, Institute of Child Health and Hospital for Children, Chennai, India)
,
Auerbach Arleen D.
(Human Genetics and Hematology Program, The Rockefeller University, New York, New York)
,
Takata Minoru
(Laboratory of DNA Damage Signaling, Department of Late Effects Studies, Radiation Biology Centre, Graduate School of Biostudies, Kyoto University, Kyoto, Japan)
,
Chandrasekharappa Settara C.
(Cancer Genomics Unit, Cancer Genetics and Comparative Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland)
,
Vundinti Babu Rao
(Department of Cytogenetics, National Institute of Immunohaematology (ICMR), Mumbai, Maharashtra, India)
資料名:
Human Mutation
(Human Mutation)
巻:
41
号:
1
ページ:
122-128
発行年:
2020年
JST資料番号:
W2601A
ISSN:
1059-7794
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
アメリカ合衆国 (USA)
言語:
英語 (EN)