Mlitochondrial Disorders in Pediatrics: Clinical, Biochemical, and Genetic Implications  

Oleh:

Clarke, Lorne A

Jenis: Article from Journal - ilmiah internasional
Dalam koleksi: Pediatric Clinics of North America vol. 39 no. 02 (Apr. 1992), page 319.

Ketersediaan

Perpustakaan FK Nomor Panggil: P13.K.1992.02 Non-tandon: 1 (dapat dipinjam: 0) Tandon: tidak ada

Lihat Detail Induk

Isi artikel

The “mitochondrial diseases” represent a unique group of metabolic disorders that challenge the classic approaches to inborn errors of metabolism. The clinical, biochemical, and genetic phenotypes of these disorders are varied and cover almost all areas of pediatrics.

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