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Nature Genetics|February 1, 1996
Brca1 deficiency results in early embryonic lethality characterized by neuroepithelial abnormalitiesL C Gowen, B L Johnson, A M Latour, et al.Nature Genetics|February 1, 1996
Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorptionM G Martín, E Turk, M P Lostao, et al.Nature Genetics|August 1, 1996
Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndromeK A Przylepa, W Paznekas, M Zhang, et al.Nature Genetics|May 1, 1996
The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3G A Nicholson, J L Dawkins, I P Blair, et al.Nature Genetics|May 1, 1996
Genetic analysis of ageing: role of oxidative damage and environmental stressesG M Martin, S N Austad, T E JohnsonNature Genetics|May 1, 1996
Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injuryA G Reaume, J L Elliott, E K Hoffman, et al.Nature Genetics|May 1, 1996
Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscleK Poetter, H Jiang, S Hassanzadeh, et al.Nature Genetics|May 1, 1996
A R59W mutation in human protoporphyrinogen oxidase results in decreased enzyme activity and is prevalent in South Africans with variegate porphyriaP N Meissner, T A Dailey, R J Hift, et al.Nature Genetics|July 1, 1996
Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox geneQ Zhao, R R Behringer, B de CrombruggheNature Genetics|July 1, 1996
A single mouse gene encodes the mitochondrial transcription factor A and a testis-specific nuclear HMG-box proteinN G Larsson, J D Garman, A Oldfors, et al.Pageof 744