Mutation rate in Duchenne type of muscular dystrophy.

Journal of medical genetics ·Vol. 7 ·No. 4 ·1970-12-00 ·Pages 334-7

Gardner-Medwin D

Abstract

暂无摘要

MeSH Terms

Child, Preschool Counseling Creatine Kinase/blood Female Heterozygote Humans Infant Male Muscular Dystrophies/genetics Mutation

Chemicals

Creatine Kinase

Authors & Affiliations

1 authors, click to expand affiliations / ORCID

Gardner-Medwin D

References (8)

8 references, click to expand

Benign spinal muscular atrophy arising in childhood and adolescence.
J Neurol Sci. 1967 Jul-Aug;5(1):121-58 PMID: 6061756
Studies in disorders of muscle. V. The inheritance of childhood progressive muscular dystrophy in 33 kindreds.
Am J Hum Genet. 1951 Jun;3(2):111-25 PMID: 14902757
Muscular dystrophy in childhood; the genetic aspect; a field study in the Leeds region of clinical types and their inheritance.
Ann Hum Genet. 1959 Apr;23(2):127-63 PMID: 13637556
An assessment of the creatine kinase test in the detection of carriers of Duchenne muscular dystrophy.
J Pediatr. 1967 Jul;71(1):82-93 PMID: 5293863
Formal genetics of muscular dystrophy.
Am J Hum Genet. 1959 Dec;11:360-79 PMID: 14424475
On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies.
Ann Hum Genet. 1955 Aug;20(1):1-38 PMID: 13249224
Muscular dystrophy in Northern Ireland. IV. Some additional data.
Ann Hum Genet. 1958 May;22(3):231-4 PMID: 13534208
The cardiomyopathy of progressive muscular dystrophy.
Circulation. 1966 Apr;33(4):625-48 PMID: 5937560

Article Info

Journal

Journal of medical genetics

Abbr.

J Med Genet

ISSN

0022-2593

DOI

Published

1970-12-00

Pages

334-7

Language

English

Region

England

NLM ID

2985087R

PMCID

PMC1468933

Subset

External Links

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