Two novel mutations in the lactase gene in a Japanese infant with congenital lactase deficiency.

Uchida, Nao; Sakamoto, Osamu; Irie, Masahiro; Abukawa, Daiki; Takeyama, Junji; Kure, Shigeo; Tsuchiya, Shigeru

Uchida, Nao; Sakamoto, Osamu; Irie, Masahiro; Abukawa, Daiki; Takeyama, Junji; Kure, Shigeo; Tsuchiya, Shigeru.

Affiliation

Uchida N; Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan. nao-uchida@umin.ac.jp

Tohoku J Exp Med ; 227(1): 69-72, 2012 05.

Article in En | MEDLINE | ID: mdl-22688420

Subject(s)

Lactase/genetics; Lactose Intolerance/genetics; Base Sequence; Blood Glucose/analysis; Female; Humans; Infant, Newborn; Japan; Lactose/administration & dosage; Lactose Intolerance/pathology; Molecular Sequence Data; Mutation, Missense/genetics; Sequence Analysis, DNA; Sequence Deletion/genetics

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Database: MEDLINE Main subject: Lactase / Lactose Intolerance Limits: Female / Humans / Newborn Country/Region as subject: Asia Language: En Journal: Tohoku J Exp Med Year: 2012 Type: Article Affiliation country: Japan

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