The first pediatric case of glucagon receptor defect due to biallelic mutations in is identified by newborn screening of elevated arginine
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The first pediatric case of glucagon receptor defect due to biallelic mutations in is identified by newborn screening of elevated arginine
description
wetenschappelijk artikel
@nl
наукова стаття, опублікована в грудні 2018
@uk
name
The first pediatric case of gl ...... screening of elevated arginine
@en
The first pediatric case of gl ...... screening of elevated arginine
@nl
type
label
The first pediatric case of gl ...... screening of elevated arginine
@en
The first pediatric case of gl ...... screening of elevated arginine
@nl
altLabel
The first pediatric case of gl ...... screening of elevated arginine
@en
prefLabel
The first pediatric case of gl ...... screening of elevated arginine
@en
The first pediatric case of gl ...... screening of elevated arginine
@nl
P2093
P2860
P1476
The first pediatric case of gl ...... screening of elevated arginine
@en
P2093
Doris O Fadoju
J Nina Ham
Lihua Zhao
Lora J H Bean
Michael J Gambello
Rani Singh
P2860
P356
10.1016/J.YMGMR.2018.09.006
P407
P577
2018-12-01T00:00:00Z