Associated Papers
Case report: Two unique nonsense mutations in HTRA1-related cerebral small vessel disease in a Chinese population and literature review.
Chen W et al.
Frontiers in Neurology, 2022
36619910 (PubMed )
Supplement: Data_Sheet_3.ZIP › case-C › 3.________ › CA2245B________.__________________________________.xlsx › sheet1
Frequent mutation of hypoxia-related genes in persistent pulmonary hypertension of the newborn.
Wang M et al.
Respiratory Research, 2020
32054482 (PubMed )
Supplement: 12931_2020_1314_MOESM1_ESM.xlsx › S6
Favourable response to ketogenic dietary therapies: undiagnosed glucose 1 transporter deficiency syndrome is only one factor.
Schoeler NE et al.
Developmental Medicine and Child Neurology, 2015
Select a paper to view details