Werdnig Hoffman'S Disease (Spinal Muscular Atrophy Type I): A Clinical Study of 25 Saudi Nationals in Al-Khobar-Reference-Cited by-同舟云学术

Werdnig Hoffman'S Disease (Spinal Muscular Atrophy Type I): A Clinical Study of 25 Saudi Nationals in Al-Khobar

Published:1992-01 Issue:1 Volume:12 Page:67-71
ISSN:0256-4947
Container-title:Annals of Saudi Medicine
language:en
Short-container-title:Ann Saudi Med

Author:

Al-Rajeh Saad¹,Bademosi Olajide¹,Gascon Generoso G.²,Stumpf David³

Affiliation:

1. From the Department of Neurology, Northwestern University Medical School and Children's Memorial Hospital, Chicago, Illinois, U.S.A.

2. From the King Faisal University, Dammam, Department of Pediatrics, Northwestern University Medical School and Children's Memorial Hospital, Chicago, Illinois, U.S.A.

3. From the King Faisal Specialist Hospital and Research Centre, Riyadh, and Department of Pediatrics and Neurology, Northwestern University Medical School and Children's Memorial Hospital, Chicago, Illinois, U.S.A.

Publisher

King Faisal Specialist Hospital and Research Centre

Subject

General Medicine

Reference28 articles.

1. Genetic mapping of chronic childhood onset spinal muscular atrophy to chromosome 5q11.2-13.3;Brzustowiz LM;Nature,1990

2. Mapping of acute (type 1) spinal muscular atrophy to chromosome 5q12-q14;Melki G;Lancet,1990

3. Phenotypic heterogeneity of SMA mapping to chromosome 5q11.1-13.3 (SMA 5q);Munsat TL;Neurology

4. Classification of the spinal muscular atrophies;Pearn J;Lancet,1980

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