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Neurogenetics. 1998 Dec;2(1):55-60.

Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers.

Author information

1
Northwestern University Medical School, Tarry Building Room 13-715, 300 E. Superior Street, Chicago, Illinois 60611, USA. afif@nwu.edu

Abstract

Autosomal recessive familial amyotrophic lateral sclerosis (RFALS) is a rare form of ALS that usually presents at an early age with slow progression of symptoms. RFALS is clinically and genetically heterogeneous and the locus of RFALS type 3 was mapped to 2q33 (ALS2) in a single family. We now report linkage of a more-common form of RFALS to chromosome 15q15-q22 markers (ALS5) and show further genetic locus heterogeneity in RFALS. ALS5 is the locus for most families with RFALS and appears to be present in both North African and European populations.

PMID:
9933301
DOI:
10.1007/s100480050052
[Indexed for MEDLINE]

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