Literature DB >> 5278749

Type IV glycogen storage disease: branching enzyme deficiency in skin fibroblasts and possible heterozygote detection.

R R Howell, M M Kaback, B I Brown.   

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Year:  1971        PMID： 5278749     DOI： 10.1016/s0022-3476(71)80466-3

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  4 in total

Review 1.  Inborn errors of metabolism: principles and their applications.

Authors:  L Pinksy
Journal:  Can Med Assoc J       Date:  1972-03-18       Impact factor: 8.262

2.  Juvenile hereditary polyglucosan body disease with complete branching enzyme deficiency (type IV glycogenosis).

Authors:  J M Schröder; R May; Y S Shin; M Sigmund; S Nase-Hüppmeier
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

3.  A juvenile variant of glycogenosis IV (Andersen disease).

Authors:  A S Guerra; O P van Diggelen; F Carneiro; R M Tsou; S Simoes; N T Santos
Journal:  Eur J Pediatr       Date:  1986-08       Impact factor: 3.183

4.  Branching enzyme activity of cultured amniocytes and chorionic villi: prenatal testing for type IV glycogen storage disease.

Authors:  B I Brown; D H Brown
Journal:  Am J Hum Genet       Date:  1989-03       Impact factor: 11.025
  4 in total

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