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Identification of TMEM230 mutations in familial Parkinson's diseaseThe KCNH2 genetic polymorphism (1956, C>T) is a novel biomarker that is associated with CCB and α,β-ADR blocker response in EH patients in ChinaA novel COL4A5 mutation identified in a Chinese Han family using exome sequencingExome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly.Comparing the role of glutathione-S-transferase and mitochondrial aldehyde dehydrogenase in nitroglycerin biotransformation and the correlation with calcitonin gene-related peptide.Pharmacokinetics of rosuvastatin when coadministered with rifampicin in healthy males: a randomized, single-blind, placebo-controlled, crossover study.OATP1B1 POLYMORPHISM IS A MAJOR DETERMINANT OF SERUM BILIRUBIN LEVEL BUT NOT ASSOCIATED WITH RIFAMPICIN-MEDIATED BILIRUBIN ELEVATIONOrganic anion transporting polypeptide-1B1 haplotypes in Chinese patientsSystematic analysis of genetic variants in patients with essential tremor
P50
Q28115600-799ACDC9-278A-40D7-B20C-84A1C5352FADQ28486352-396625B7-34DF-4CB4-A91C-6DFD169DF2C2Q33943303-531669BF-ECEA-4D04-964F-D23961653F0CQ36029016-2867DFFC-E33F-43D3-BEC6-088EEDFD88ADQ45940306-A1493540-3810-477E-A588-E9FEDCBF61B9Q46436953-2471C09B-BF30-4E50-9710-357E8E0DE305Q57500316-8DF5B4A8-9FE3-4FEB-880B-F09532C9113BQ57500318-D4B6801C-C67C-4AD8-8BED-E54F16CC99B9Q58762277-75CAD7FB-36C4-430C-B12A-3769A511897D
P50
description
researcher ORCID ID = 0000-0002-8313-6522
@en
name
Sheng Deng
@ast
Sheng Deng
@en
Sheng Deng
@es
Sheng Deng
@nl
type
label
Sheng Deng
@ast
Sheng Deng
@en
Sheng Deng
@es
Sheng Deng
@nl
prefLabel
Sheng Deng
@ast
Sheng Deng
@en
Sheng Deng
@es
Sheng Deng
@nl
P1153
19336794900
P31
P496
0000-0002-8313-6522