Tuberous Sclerosis Complex in Chinese patients: Phenotypic analysis and mutational screening of TSC1/TSC2 genes-Reference-Cited by-同舟云学术

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Tuberous Sclerosis Complex in Chinese patients: Phenotypic analysis and mutational screening of TSC1/TSC2 genes

Published:2019-10 Issue: Volume:71 Page:322-327
ISSN:1059-1311
Container-title:Seizure
language:en
Short-container-title:Seizure

Author:

Lin Shan,Zeng Jia-Bin,Zhao Gui-Xian,Yang Zhen-Zhen,Huang Hui-Ping,Lin Min-Ting,Wu Zhi-Ying,Wang Ning,Chen Wan-Jin,Fang Ling

Funder

Natural Science Foundation of Fujian Province, China

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology,General Medicine

Reference37 articles.

1. Genotype/phenotype correlations in tuberous sclerosis complex;Curatolo;Semin Pediatr Neurol,2015

2. The genomic landscape of tuberous sclerosis complex;Martin;Nat Commun,2017

3. Identification and characterization of the tuberous sclerosis gene on chromosome 16;Consortium;Cell,1993

4. Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34;Slegtenhorst;Science,1997

5. Mammalian target of rapamycin inhibitors and life-threatening conditions in tuberous sclerosis complex;Moavero;Semin Pediatr Neurol,2015

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1. Clinical practice recommendations for kidney involvement in tuberous sclerosis complex: a consensus statement by the ERKNet Working Group for Autosomal Dominant Structural Kidney Disorders and the ERA Genes & Kidney Working Group;Nature Reviews Nephrology;2024-03-05

2. Bibliometric analysis and network visualization on Tuberous Sclerosis Complex;Bangladesh Journal of Medical Science;2024-01-02

3. Tsc2 mutation rather than Tsc1 mutation dominantly causes a social deficit in a mouse model of tuberous sclerosis complex;Human Genomics;2023-02-02

4. Tsc2 mutation rather than Tsc1 mutation dominantly causes a social deficit in a mouse model of tuberous sclerosis complex;2022-10-31

5. Genotype/phenotype correlation in 123 Chinese patients with Tuberous Sclerosis Complex;European Journal of Medical Genetics;2022-10

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