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Keyword [SCN4A]
Result: 1 - 11 | Page: 1 of 1
1.
Genetic Research Of Disease-related Mutations And Clinical Study On Periodic Paralyses
2.
Genetic Research Of Ion Channel Gene Mutations And Clinical Study On Primary Hypokalemic Periodic Paralysis
3.
Value Of Exercise Test In The Diagnosis Of Patients With Periodic Paralysis
4.
SCN4A Gene Mutations Analysis In Normokalemic Periodic Paralysis Patients
5.
The Clinical And Gene Mutation Study In A Large Family Of Paramyotonia Congenita
6.
Analysis Of Mutation In Gene CACNA1S And SCN4A Of The Hypokalemic Periodic Paralysis Pedigree
7.
Gene Sequence Analysis Of Hypokalemic Periodic Paralysis Patients In A Family
8.
Gene Analysis Of The Hypokalemic Periodic Paralysis Pedigree
9.
Clinical Characteristics Of Hypokalemic Periodic Paralysis And Genes Screening Of CACNA1S And SCN4A In Hypokalemic Periodic Paralysis
10.
The Clinical Features And Mutation Analysis Of SCN4A Gene In A Normokalemic Periodic Paralysis Family
11.
N1366S Mutation Of Human Skeletal Muscle Sodium Channel Causes Paramyotonia Congenita
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