Branched chain acyltransferase absence due to an Alu-based genomic deletion allele and an exon skipping allele in a compound heterozygote proband expressing maple syrup urine disease.

No abstract is available for this paper.

• Publication year

  1992

• Venue

  Biochimica et Biophysica Acta

• Publication date

  1992-03-20

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/0925-4439(92)90043-MPMID 1547285
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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