Spinal muscular atrophy is not the result of mutations of the beta-hexosaminidase or GM2-activator locus

Journal article

Peer reviewed

P. W Kleyn, L. M Brzustowicz, K. C Wilhelmsen, N. B Freimer, J. M Miller, T. L Munsat and T. C Gillian

Neurology, Vol.41(9), pp.1418-1422

1991

PMID: 1679910

Abstract

Biological and medical sciences

Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases

Medical sciences

Neurology

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Title: Spinal muscular atrophy is not the result of mutations of the beta-hexosaminidase or GM2-activator locus
Creators: P. W Kleyn - Columbia univ., dep. psychiatry, New York NY 10032, United States
L. M Brzustowicz - Columbia univ., dep. psychiatry, New York NY 10032, United States
K. C Wilhelmsen - Columbia univ., dep. psychiatry, New York NY 10032, United States
N. B Freimer - Columbia univ., dep. psychiatry, New York NY 10032, United States
J. M Miller - Columbia univ., dep. psychiatry, New York NY 10032, United States
T. L Munsat - Columbia univ., dep. psychiatry, New York NY 10032, United States
T. C Gillian - Columbia univ., dep. psychiatry, New York NY 10032, United States
Publication Details: Neurology, Vol.41(9), pp.1418-1422
Date published: 1991
Publisher: Lippincott Williams & Wilkins
Academic Unit: Human Genetics Institute of New Jersey; Genetics (SAS)
Language: English
Resource Type: Journal article
Identifiers: 991031666242804646