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Keyword [SLC33A1]
Result: 1 - 6 | Page: 1 of 1
1.
Clinical Features And Identification Of The Disease-Causing Genes In The Kindreds Of Hereditary Spastic Paraplegia And Charcot-Marie-Tooth Disease
2.
Research On The Function And The Underlying Mechanism Of SPG42Causative Gene SLC33A1
3.
Identification And Function Analysis Of Hereditary Spastic Paraplegia Causative Gene SLC33A1 Mutation Site C.339T>G (p.Ser113Arg)
4.
S113R Mutation In Slc33a1 Leads To Hereditary Spastic Paraplegia And Augmented BMP Signaling In A Mouse Model
5.
A Preliminary Research On The Effect Of Hereditary Spastic Paraplegia Causatave Gene SLC3A1 Missense Mutation On Mitochondria
6.
The Differential Expression Of SLC33A1 Gene In Peripheral Blood May Serve As A Genetic Marker For The Diagnosis Of Coronary Heart Disease
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