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Lack of meaningful genotype-phenotype association in SCN1A-related infantile-onset epileptic encephalopathies
Lack of meaningful genotype-phenotype association in SCN1A-related infantile-onset epileptic encephalopathies
2017
Siti Aishah Abdul Wahab
Yusnita Yakob
Teik Beng Khoo
Sangita Dharshini Terumalay
Vigneswari Ganesan
Chee Ming Teh
Nor Azni bin Yahaya
Hock Sin Heng
Manonmani Vaithialingam
Sau Wei Wong
Keywords:
Immunology
Pathology
Genotype-Phenotype Association
Diabetes mellitus
Infantile onset
Medicine
genotype phenotype
Correction
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