Combination of thrombocytopenia and hypocalcemia may indicate the possibility of Stormorken Syndrome with STIM1 mutation
Saved in:
Main Authors: | Chen-Hua Wang (Author), Wen-Chen Liang (Author), Pei-Chin Lin (Author), Yuh-Jyh Jong (Author) |
---|---|
Format: | Book |
Published: |
Elsevier,
2022-03-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Life-threatening Dilated Cardiomyopathy Induced by Late-onset Neonatal Hypocalcemia
by: Po-Ching Chou, et al.
Published: (2016) -
Association of pregnancy hypocalcemia and neonatal growth indices
by: Sima Hashemipour, et al.
Published: (2018) -
Limb-girdle Muscular Dystrophy Type 2A with Mutation in CAPN3: The First Report in Taiwan
by: Chien-Hua Wang, et al.
Published: (2015) -
Case Report: Novel TRPM6 Mutations Cause Hereditary Hypomagnesemia With Secondary Hypocalcemia in a Chinese Family and a Literature Review
by: Yiran Han, et al.
Published: (2022) -
Expression of Orai1 and STIM1 in human oral squamous cell carcinogenesis
by: Yen-Yun Wang, et al.
Published: (2022)