PDGFRB mutation causes autosomal-dominant Penttinen syndrome

PDGFRB mutation causes autosomal-dominant Penttinen syndrome

10.1111/cge.12680

Saved in:
Bibliographic Details
Main Author: Aminkeng, F
Other Authors: MEDICINE
Format: Article
Language:English
Published: WILEY-BLACKWELL 2022
Subjects:
Science & Technology
Life Sciences & Biomedicine
Genetics & Heredity
Online Access:https://scholarbank.nus.edu.sg/handle/10635/235098
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: National University of Singapore
Language: English
id sg-nus-scholar.10635-235098
record_format dspace
spelling sg-nus-scholar.10635-2350982024-04-17T08:36:34Z PDGFRB mutation causes autosomal-dominant Penttinen syndrome Aminkeng, F MEDICINE Science & Technology Life Sciences & Biomedicine Genetics & Heredity 10.1111/cge.12680 CLINICAL GENETICS 88 6 531-U7 2022-12-01T08:33:53Z 2022-12-01T08:33:53Z 2015-12-01 2022-11-30T18:48:26Z Article Aminkeng, F (2015-12-01). PDGFRB mutation causes autosomal-dominant Penttinen syndrome. CLINICAL GENETICS 88 (6) : 531-U7. ScholarBank@NUS Repository. https://doi.org/10.1111/cge.12680 0009-9163 1399-0004 https://scholarbank.nus.edu.sg/handle/10635/235098 en WILEY-BLACKWELL Elements
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
language English
topic Science & Technology
Life Sciences & Biomedicine
Genetics & Heredity
spellingShingle Science & Technology
Life Sciences & Biomedicine
Genetics & Heredity
Aminkeng, F
PDGFRB mutation causes autosomal-dominant Penttinen syndrome
description 10.1111/cge.12680
author2 MEDICINE
author_facet MEDICINE
Aminkeng, F
format Article
author Aminkeng, F
author_sort Aminkeng, F
title PDGFRB mutation causes autosomal-dominant Penttinen syndrome
title_short PDGFRB mutation causes autosomal-dominant Penttinen syndrome
title_full PDGFRB mutation causes autosomal-dominant Penttinen syndrome
title_fullStr PDGFRB mutation causes autosomal-dominant Penttinen syndrome
title_full_unstemmed PDGFRB mutation causes autosomal-dominant Penttinen syndrome
title_sort pdgfrb mutation causes autosomal-dominant penttinen syndrome
publisher WILEY-BLACKWELL
publishDate 2022
url https://scholarbank.nus.edu.sg/handle/10635/235098
_version_ 1800915744487112704

Similar Items