Metachromatic leukodystrophy: A novel mutation (c237delC) and extension of the haplotype associated with the P426L mutation

No abstract is available for this paper.

• Publication year

  2000

• Venue

  Human Mutation

• Publication date

  2000-10-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1002/1098-1004(200010)16:4<375::AID-HUMU21>3.0.CO;2-CPMID 11013459
• 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.

• No references are available for this paper.

• Metachromatic leukodystrophy

  2018cites this paper
• Mutation Update of ARSA and PSAP Genes Causing Metachromatic Leukodystrophy

  2016cites this paper
• Leukodystrophies: recent developments in genetics, molecular biology, pathogenesis and treatment*

  2001cites this paper