Corpus 1,272 assessed · 1,173 scored · 643 reproduced ≥75 · 168 flagged ·∅ 74.1/100

Publications 2 Datasets 392.5k Experiments 4.7k

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Filters: University Medical Center Hamburg-Eppendorf ✕ Reproducible only ✕ sanger sequencing ✕ clear all

2 matching publication(s)

Publication	Journal	Year	Score	Verdict
Exome sequencing in 38 patients with intracranial aneurysms and subarachnoid hemorrhage. ⚑ PMID 32367296	—	2020	78	78/100 ⚑
An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndrome. PMID 24781758	—	2015	83	L1 83/100

Exome sequencing in 38 patients with intracranial aneurysms and subarachnoid hemorrhage.⚑

PMID 32367296 · · 2020

78/100 ⚑

An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndrome.

PMID 24781758 · · 2015

L1 83/100