Biotinidase deficiency--a treatable entity. | Indian J Pediatr; 2000 Jun; 67(6): 464-6 | IMSEAR

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Biotinidase deficiency--a treatable entity.

Gulati, S; Passi, G R; Kumar, A; Kabra, M; Kalra, V; Verma, I C.

Indian J Pediatr ; 2000 Jun; 67(6): 464-6

Article in En | IMSEAR | ID: sea-79547

Subject(s)

Amidohydrolases/deficiency; Biotin/therapeutic use; Biotinidase; Humans; Infant; Male; Metabolism, Inborn Errors/complications; Nervous System Diseases/etiology; Prognosis

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Full text: 1 Index: IMSEAR Main subject: Prognosis / Biotin / Humans / Male / Biotinidase / Amidohydrolases / Infant / Metabolism, Inborn Errors / Nervous System Diseases Type of study: Prognostic_studies / Screening_studies Language: En Journal: Indian J Pediatr Year: 2000 Type: Article

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Full text: 1 Index: IMSEAR Main subject: Prognosis / Biotin / Humans / Male / Biotinidase / Amidohydrolases / Infant / Metabolism, Inborn Errors / Nervous System Diseases Type of study: Prognostic_studies / Screening_studies Language: En Journal: Indian J Pediatr Year: 2000 Type: Article