文献
J-GLOBAL ID:202002230594853257
整理番号:20A0974165
TWNK遺伝子関連Perrault症候群の表現型の拡大【JST・京大機械翻訳】
Broadening the phenotype of the TWNK gene associated Perrault syndrome
著者 (10件):
Fekete Balint
(Institute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary)
,
Pentelenyi Klara
(Institute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary)
,
Rudas Gabor
(MR Research Centre, Semmelweis University, Budapest, Hungary)
,
Gal Aniko
(Institute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary)
,
Grosz Zoltan
(Institute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary)
,
Illes Anett
(Institute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary)
,
Idris Jimoh
(Institute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary)
,
Csukly Gabor
(Department of Psychiatry and Psychotherapy, Semmelweis University, Budapest, Hungary)
,
Domonkos Andor
(Institute of Experimental Medicine of the Hungarian Academy of Sciences, Budapest, Hungary)
,
Molnar Maria Judit
(Institute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary)
資料名:
BMC Medical Genetics (Web)
(BMC Medical Genetics (Web))
巻:
20
号:
1
ページ:
1-8
発行年:
2019年
JST資料番号:
U7307A
ISSN:
1471-2350
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
イギリス (GBR)
言語:
英語 (EN)