The gene frequency of acute Werdnig-Hoffmann disease (SMA type 1). A total population survey in North-East England.

Journal of medical genetics ·Vol. 10 ·No. 3 ·1973-09-00 ·Pages 260-5

Pearn JH

Abstract

暂无摘要

MeSH Terms

Acute Disease Birth Rate Child, Preschool Demyelinating Diseases/genetics England Female Gene Frequency Humans Infant Infant, Newborn Male Methods Motor Neurons Muscular Atrophy/epidemiology,genetics Paralysis/genetics Spinal Cord Diseases/epidemiology,genetics

Authors & Affiliations

1 authors, click to expand affiliations / ORCID

Pearn J H

References (10)

10 references, click to expand

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A new genetic variant of the spinal muscular atrophies in infancy.
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Adenosine deaminase (ADA) polymorphism in Northern England.
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Article Info

Journal

Journal of medical genetics

Abbr.

J Med Genet

ISSN

0022-2593

DOI

10.1136/jmg.10.3.260

Published

1973-09-00

Pages

260-5

Language

English

Region

England

NLM ID

2985087R

PMCID

PMC1013030

Subset

External Links

PubMed source DOI: 10.1136/jmg.10.3.260 PMC Full Text View journal details

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The gene frequency of acute Werdnig-Hoffmann disease (SMA type 1). A total population survey in North-East England.

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