(Q28295776)

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Richner-Hanhart syndrome (tyrosinemia type II). Case report and literature review

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title

Richner-Hanhart syndrome (tyrosinemia type II). Case report and literature review (English)

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A I al-Hemidan

1

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S A al-Hazzaa

series ordinal

2

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language of work or name

English

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publication date

March 1995

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published in

Ophthalmic Genetics

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volume

16

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issue

1

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page(s)

21-6

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cites work

Soluble and mitochondrial forms of tyrosine aminotransferase. Relationship to human tyrosinemia.

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https://api.crossref.org/works/10.3109%2F13816819509057850

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21 January 2018

Metabolic studies on two patients with nonhepatic tyrosinemia using deuterated tyrosine loads

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https://api.crossref.org/works/10.3109%2F13816819509057850

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21 January 2018

Assignment of the human tyrosine aminotransferase gene to chromosome 16.

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reference URL

https://api.crossref.org/works/10.3109%2F13816819509057850

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21 January 2018

Familial tyrosinaemia with eye and skin lesions. Presentation of two cases

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https://api.crossref.org/works/10.3109%2F13816819509057850

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21 January 2018

The effect of diet on the ophthalmological, clinical and biochemical aspects of Richner-Hanhart syndrome: a morphological ultrastructural study of the cornea and the conjunctiva.

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21 January 2018

Conrneal tyrosine crystals in transient neonatal tyrosinemia

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21 January 2018

The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22?q24) by somatic cell hybrid analysis and in situ hybridization

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reference URL

https://api.crossref.org/works/10.3109%2F13816819509057850

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21 January 2018

Identifiers

DOI

10.3109/13816819509057850

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PubMed publication ID

7648039

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(Q28295776)

Richner-Hanhart syndrome (tyrosinemia type II). Case report and literature review

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