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glycogenolysis
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Pierpont syndrome due to mutation c.1337A > G in TBL1XR1 gene
Publication at First Faculty of Medicine
|
2022
7 people
Abstract
Here we report the case of a boy whose parents are healthy and older siser has celiac disease.
Keywords
developmental delay
plantar lipomatosis
activation
spectrum
deletion
People
person
RNDr. Hana Hansíková CSc.
First Faculty of Medicine
person
MUDr. Alena Leiská
First Faculty of Medicine
person
prof. MUDr. Jiří Zeman DrSc.
First Faculty of Medicine
person
prof. MUDr. Ing. Lukáš Lambert Ph.D.
First Faculty of Medicine
person
Mgr. Alžběta Vondráčková Ph.D.
First Faculty of Medicine
person
doc. MUDr. Alice Baxová CSc.
First Faculty of Medicine
person
Ing. Markéta Tesařová Ph.D.
First Faculty of Medicine