SCOPUS 정보 검색 플랫폼

Volumn 37, Issue 3, 2001, Pages 624-628

Holoprosencephaly and low molecular weight proteinuria: The human homologue of murine megalin deficiency

(7) Müller, Dominik a,b,c,d Ankermann, Tobias a,b,c,d Stephani, Ulrich a,b,c,d Kirschstein, Martin a,b,c,d Szelestei, Tamas a,b,c,d Luft, Friedrich C a,e Willnow, Thomas E a,b,c,d

a UNIVERSITY OF KIEL (Germany)

b Children's Hospital (Germany)

c HUMBOLDT UNIVERSITY (Germany)

d MAX DELBRÜCK CENTER FOR MOLECULAR MEDICINE (Germany)

e FRANZ VOLHARD CLINIC (Germany)

Author keywords

Fanconi's syndrome; Genetics; Holoprosencephaly; Megalin; Tubular proteinuria; Tubulopathy; Vitamin D

Indexed keywords

ALBUMIN; LOW DENSITY LIPOPROTEIN RECEPTOR; MEGALIN; VITAMIN D; VITAMIN D BINDING PROTEIN;

ARTICLE; CASE REPORT; FEMALE; GENE LOCUS; HAPLOTYPE; HOLOPROSENCEPHALY; HUMAN; INFANT; KIDNEY TUBULE DISORDER; LUNG INSUFFICIENCY; MEGALIN DEFICIENCY; PHENOTYPE; PROTEIN DEFECT; PROTEIN DEFICIENCY; PROTEINURIA; URINARY EXCRETION; VITAMIN D METABOLISM;

EID: 0035127319 PISSN: 02726386 EISSN: None Source Type: Journal
DOI: 10.1053/ajkd.2001.22092 Document Type: Article

Times cited : (15)

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