Ishiura H

References (3)

Title : A novel homozygous nonsense variant of LMF1 in pregnancy-induced hypertriglyceridemia with acute pancreatitis - Tanaka_2023_J.Clin.Lipidol__
Author(s) : Tanaka M , Takase S , Ishiura H , Yamauchi T , Okazaki S , Okazaki H
Ref : J Clin Lipidol , : , 2023
Abstract :
PubMedSearch : Tanaka_2023_J.Clin.Lipidol__
PubMedID: 37005154

Title : VPS13D-related disorders presenting as a pure and complicated form of hereditary spastic paraplegia - Koh_2020_Mol.Genet.Genomic.Med_8_e1108
Author(s) : Koh K , Ishiura H , Shimazaki H , Tsutsumiuchi M , Ichinose Y , Nan H , Hamada S , Ohtsuka T , Tsuji S , Takiyama Y
Ref : Mol Genet Genomic Med , 8 :e1108 , 2020
Abstract :
PubMedSearch : Koh_2020_Mol.Genet.Genomic.Med_8_e1108
PubMedID: 31876103

Title : Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses - Ishiura_2014_J.Hum.Genet_59_163
Author(s) : Ishiura H , Takahashi Y , Hayashi T , Saito K , Furuya H , Watanabe M , Murata M , Suzuki M , Sugiura A , Sawai S , Shibuya K , Ueda N , Ichikawa Y , Kanazawa I , Goto J , Tsuji S
Ref : J Hum Genet , 59 :163 , 2014
Abstract :
PubMedSearch : Ishiura_2014_J.Hum.Genet_59_163
PubMedID: 24451228
Gene_locus related to this paper: human-SPG21