HOXA11 is another monogenic cause of congenital anomalies of the kidney and urinary tract—Reply

^*Corresponding author for this work

Research output: Contribution to journal › Letter › peer-review

Access to Document

@article{a4e9a66fac044666a9c628033971b400,

title = "HOXA11 is another monogenic cause of congenital anomalies of the kidney and urinary tract—Reply",

author = "Maayan Kagan and Oren Pleniceanu and Asaf Vivante",

year = "2023",

month = mar,

doi = "10.1007/s00467-022-05814-9",

language = "אנגלית",

volume = "38",

pages = "935",

journal = "Pediatric Nephrology",

issn = "0931-041X",

publisher = "Springer Verlag",

number = "3",

}

TY - JOUR

T1 - HOXA11 is another monogenic cause of congenital anomalies of the kidney and urinary tract—Reply

AU - Kagan, Maayan

AU - Pleniceanu, Oren

AU - Vivante, Asaf

PY - 2023/3

Y1 - 2023/3

UR - http://www.scopus.com/inward/record.url?scp=85142175685&partnerID=8YFLogxK

U2 - 10.1007/s00467-022-05814-9

DO - 10.1007/s00467-022-05814-9

M3 - ???researchoutput.researchoutputtypes.contributiontojournal.letter???

C2 - 36401625

AN - SCOPUS:85142175685

SN - 0931-041X

VL - 38

SP - 935

JO - Pediatric Nephrology

JF - Pediatric Nephrology

IS - 3

ER -