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Links from PubMed

Items: 5

1.

Novel mutations in the homogentisate-1,2-dioxygenase gene identified in Slovak patients with alkaptonuria.

Zatková A, Polaková H, Micutková L, Zvarík M, Bosák V, Feráková E, Matusek J, Ferák V, Kádasi L.

J Med Genet. 2000 Jul;37(7):539-42. No abstract available.

2.

Alkaptonuria in Slovakia: thirty-two years of research on phenotype and genotype.

Srsen S, Müller CR, Fregin A, Srsnova K.

Mol Genet Metab. 2002 Apr;75(4):353-9. Review.

PMID:
12051967
3.

Are we ready to try to cure alkaptonuria?

La Du BN Jr.

Am J Hum Genet. 1998 Apr;62(4):765-7. Review. No abstract available.

4.

[Alkaptonuria (homogentisic aciduria)].

Takita H.

Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):328-31. Review. Japanese. No abstract available.

PMID:
9590059
5.

[Molecular-genetic analysis of hereditary neurological diseases].

Slominskiĭ PA.

Mol Biol (Mosk). 1999 Jan-Feb;33(1):74-9. Review. Russian. No abstract available.

PMID:
10330663

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