Menkes disease [6] (multiple letters)

Ophthalmology

Volumn 106, Issue 3, 1999, Pages 442-443

  Gasch, A T ^a   Kaler, S G ^a   Kaiser Kupfer, M ^a   Bateman, J B ^a   Ferreira, R C ^a   Heckenlively, J R ^a   Menkes, J ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL ARTICLE; DISEASE ASSOCIATION; GENE MUTATION; HOMEOBOX; HUMAN; IRIS; LETTER; MENKES SYNDROME; PRIORITY JOURNAL; CONGENITAL MALFORMATION; EYE MALFORMATION; EYELASH; NOTE; RETINA DEGENERATION;

EYE ABNORMALITIES; EYELASHES; HUMANS; IRIS; MENKES KINKY HAIR SYNDROME; RETINAL DEGENERATION;

EID: 0033094191     PISSN: 01616420     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0161-6420(99)90144-6     Document Type: Letter

References (4)

1. N. Horn T. Tonnesen Z. Tumer Menkes disease an X-linked neurological disorder of the copper metabolism Brain Pathol 2 1992 351 362
2. E.V. Semina R. Reiter N.J. Leysens Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Reiger syndrome Nat Genet 14 1996 392 399
3. L.M. Alward E.V. Semina J.W. Kalenak Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene Am J Ophthalmol 125 1998 98 100
4. E.V. Semina R.S. Reiter J.C. Murray Isolation of a new homeobox gene belonging to the Pitx/Rieg family expression during lens development and mapping to the aphakia region on mouse chromosome 19 Hum Mol Genet 6 1997 2109 2116