Partial Biotinidase Deficiency

J Gordon Millichap

doi:10.15844/pedneurbriefs-4-1-6

Partial Biotinidase Deficiency

Pediatric Neurology Briefs

Volume 4 (1990): Issue 1

By: J Gordon Millichap

Open Access

|Jan 1990

Abstract

The symptoms, biochemical features and inheritance pattern of partial biotinidase deficiency have been studied at the Departments of Human Genetics and Pediatrics, Medical College of Virginia, Richmond, VA; the State Laboratory Institute, Massachusetts Department of Public Health; Massachusetts General Hospital, Boston; the Lincoln Clinic, NB; and the Division of Human Genetics, university of Maryland School of Medicine, Baltimore.

References

McVoy JRS Wolf B Levy HL Lawler M Schmidt MA Ebers DD Partial biotinidase deficiency: clinical and biochemical features J Pediatr 1990 Jan 116 1 78 83 10.1016/S0022-3476(05)81649-X 2295967
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-4-1-6 | Journal eISSN: 2166-6482

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Language: English

Page range: 6 - 7

Published on: Jan 1, 1990

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Partial Biotinidase Deficiency,

Hypotonia,

Exogenous Biotin

© 1990 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 4 (1990): Issue 1