文献
J-GLOBAL ID:201202259197640414
整理番号:12A1360862
ゲノムワイドSNPジェノタイピングによってStereocilin(STRC)遺伝子が小児両側性感音難聴の主な寄与因子として特定される
Genome-Wide SNP Genotyping Identifies the Stereocilin (STRC) Gene as a Major Contributor to Pediatric Bilateral Sensorineural Hearing Impairment
著者 (16件):
FRANCEY Lauren J.
(Children’s Hospital of Philadelphia, Pennsylvania)
,
CONLIN Laura K.
(Children’s Hospital of Philadelphia, Pennsylvania)
,
EADESCH Hanna E.
(Children’s Hospital of Philadelphia, Pennsylvania)
,
CLARK Dinah
(Children’s Hospital of Philadelphia, Pennsylvania)
,
BERRODIN Donna
(Children’s Hospital of Philadelphia, Pennsylvania)
,
SUN Yi
(Children’s Hospital of Philadelphia, Pennsylvania)
,
GLESSNER Joe
(Children’s Hospital of Philadelphia, Pennsylvania)
,
HAKONARSON Hakon
(Children’s Hospital of Philadelphia, Pennsylvania)
,
JALAS Chaim
(Bonei Olam Center for Rare Jewish Genetic Disorders, New York)
,
LANDAU Chaim
(Bonei Olam Center for Rare Jewish Genetic Disorders, New York)
,
SPINNER Nancy B.
(Children’s Hospital of Philadelphia, Pennsylvania)
,
KENNA Margaret
(Children’s Hospital Boston, Massachusetts)
,
SAGI Michal
(Hadassah-Hebrew Univ. Medical Center, Jerusalem, ISR)
,
REHM Heidi L.
(Children’s Hospital Boston, Massachusetts)
,
REHM Heidi L.
(Harvard Medical School, Massachusetts)
,
KRANTZ Ian D.
(Children’s Hospital of Philadelphia, Pennsylvania)
資料名:
American Journal of Medical Genetics. Part A
(American Journal of Medical Genetics. Part A)
巻:
158
号:
2
ページ:
298-308
発行年:
2012年02月
JST資料番号:
E0725C
ISSN:
1552-4825
資料種別:
逐次刊行物 (A)
発行国:
アメリカ合衆国 (USA)
言語:
英語 (EN)