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SDHD
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Body Atlas
Most Correlated Tissues
Skeletal muscle
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Disease Atlas
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Complete deafness
Neuroendocrine tumor
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piclamilast
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hexachlorobutadiene
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Literature
Most Relevant Literature
PALE-GREEN LEAF 1, a rice cpSRP54 protein, is essential for the assembly of the PSI-LHCI supercomple…
Differential impairment of catecholaminergic cell maturation and survival by genetic mitochondrial c…
Malignant phenotype and two SDHD mutations in a family with paraganglioma syndrome type 1.
Disomy as the genetic underlying mechanisms of loss of heterozigosity in SDHD-paragangliomas.
High prevalence of occult paragangliomas in asymptomatic carriers of SDHD and SDHB gene mutations.
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Clinical Trials
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Study Investigating MEN1 and SDHD in Familial Carcinoid Tumors
Conventional Hemodialysis Vs Short Daily Hemodialysis for Patients Coming From Peritoneal Dialysis (…
Hereditary Paraganglioma: Evaluation of Screening Methods to Detect Tumors in SDH Positive Carriers
An Investigation of Small Intestinal Carcinoid Carcinoma in Families
DFF332 as a Single Agent and in Combination With Everolimus & Immuno-Oncology Agents in Advanced/Rel…
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