A Novel Mutation in the SCN4A Gene in a Japanese Family with Paramyotonia Congenita

Satoru Takahashi, Shiho Yamamoto, Ryosuke Tanaka, Akie Okayama, Akiko Araki, Hiroki Kajino and Hiroshi Azuma

Paramyotoniacongenita is an autosomal-dominant muscle disease caused by missense mutations in SCN4A, the
gene enconding the alpha subunit of skeletal muscle sodium channe..மேலும் பார்க்க»

A Census of Premenstrual Syndrome in Young Adolescent Girls: Facts about Women Health in Developing Country

Tamseela Mumtaz, Nabila Roohi and Muhammad Amir Iqbal

Introduction: Women often experienced ragged and unpredicted kind of behavior and hardly recognize their attitude as premenstrual syndrome. Adolescent girls are..மேலும் பார்க்க»

The Resulting Advancement of Chain-End DNA Sequencing

Ning Zhao*

The transmission of qualities to a living being's posterity is the premise of the legacy of phenotypic attributes. These qualities make up various DNA arrangements called ge..மேலும் பார்க்க»

Correlation of LSPR Response and Silicon Nano-structuring of Gold Nanoparticles of Different Morphology Grown by Pulsed Laser Deposition.

Jenitta Johnson M