Liver pathology and biochemistry in patients with mutations in <scp>TRIM37</scp> gene (Mulibrey nanism)-Reference-Cited by-同舟云学术

Liver pathology and biochemistry in patients with mutations in TRIM37 gene (Mulibrey nanism)

Published:2022-03-08 Issue:6 Volume:42 Page:1369-1378
ISSN:1478-3223
Container-title:Liver International
language:en
Short-container-title:Liver International

Author:

Sivunen Johanna¹^ORCID,Karlberg Susann¹²,Kivisaari Reetta¹³,Lohi Jouko⁴,Karlberg Niklas¹,Jokinen Eero¹,Sarkola Taisto¹⁵,Jahnukainen Timo¹,Lipsanen‐Nyman Marita¹,Jalanko Hannu¹

Affiliation:

1. Children´s Hospital, University of Helsinki and Helsinki University Hospital Helsinki Finland

2. Folkhälsan Research Center Helsinki Finland

3. Department of Pediatric Radiology, HUS Medical Imaging Centre University of Helsinki and Helsinki University Hospital Helsinki Finland

4. Department of Pathology University of Helsinki Helsinki Finland

5. Minerva Foundation Institute for Medical Research Helsinki Finland

Funder

Finska Läkaresällskapet

Helsingin ja Uudenmaan Sairaanhoitopiiri

Lastentautien Tutkimussäätiö

Sigrid Juséliuksen Säätiö

Publisher

Wiley

Subject

Hepatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/liv.15213

Reference43 articles.

1. Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism

2. The TRIM37 Gene Encodes a Peroxisomal RING-B-Box-Coiled-Coil Protein: Classification of Mulibrey Nanism as a New Peroxisomal Disorder

3. Mulibrey nanism: clinical features and diagnostic criteria

4. Failure of Sexual Maturation in Mulibrey Nanism

5. Insulin Resistance Syndrome in Subjects With Mutated RING Finger Protein TRIM37

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