1. ScholarBank@NUS

XXX Folefac Aminkeng

rp62345

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Full Name
XXX Folefac Aminkeng
(not current staff)
Main Affiliation
 
Faculty
 
Email
mdcfa@nus.edu.sg
 

Publications

Refined By:
Policy:  Closed
Subject:  Genetics & Heredity

Results 1-9 of 9 (Search time: 0.005 seconds).

Issue DateTitleAuthor(s)
11-Dec-2015DLL4 loss-of-function heterozygous mutations cause Adams-Oliver syndromeAminkeng, F 
21-Sep-2014EIF2AK4 genetic mutations cause a recessive form of rare and deadly lung disease, pulmonary veno-occlusive diseaseAminkeng, F 
31-Jun-2014GFI1B mutation causes autosomal dominant gray platelet syndromeAminkeng, F 
41-Jan-2013HINT1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotoniaAminkeng, F 
51-Apr-2013KCNT1 mutations in ADNFLE and MMPSI: a new driver in the etiology and pathophysiology of early-onset epileptic syndromesAminkeng, F 
61-Jan-2013Mutations in ATP1A3 cause alternating hemiplegia of childhoodAminkeng, F 
71-Dec-2015PDGFRB mutation causes autosomal-dominant Penttinen syndromeAminkeng, F 
81-Jun-2014Using pharmacogenetics in real time to guide therapy: the warfarin exampleAminkeng, F 
91-Sep-2013WDR45 mutations define a novel disease entity - Static Encephalopathy of Childhood with Neurodegeneration in AdulthoodAminkeng, F