Literature DB >> 10771869

A case of aminolevulenic acid dehydratase deficiency porphyria (ALADP)

M N Rao, J V Shekhar, V Hussain, M Muneer.   

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Year:  1997        PMID： 10771869     DOI： 10.1007/bf02845222

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN： 0019-5456            Impact factor:   1.967


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  2 in total

1.  delta-Aminolevulinate dehydratase deficient porphyria: identification of the molecular lesions in a severely affected homozygote.

Authors:  M Plewinska; S Thunell; L Holmberg; J G Wetmur; R J Desnick
Journal:  Am J Hum Genet       Date:  1991-07       Impact factor: 11.025

2.  Enzymatic defect in a child with hereditary hepatic porphyria due to homozygous delta-aminolevulinic acid dehydratase deficiency: immunochemical studies.

Authors:  H Fujita; S Sassa; J Lundgren; L Holmberg; S Thunell; A Kappas
Journal:  Pediatrics       Date:  1987-12       Impact factor: 7.124
  2 in total

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