74th ENMC International Workshop: Mitochondrial Diseases 19-20 November 1999, Naarden, The Netherlands

Neuromuscular Disorders

Volumn 10, Issue 6, 2000, Pages 460-462

  Poulton, J ^a   Turnbull, D M ^a  

^a NEWCASTLE UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

CONFERENCE PAPER; DISORDERS OF MITOCHONDRIAL FUNCTIONS; GENETIC COUNSELING; HUMAN; MUTANT; MUTATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

DEAFNESS; DNA, MITOCHONDRIAL; GENETIC COUNSELING; HUMANS; INTERNET; LEIGH DISEASE; MELAS SYNDROME; MERRF SYNDROME; MITOCHONDRIAL MYOPATHIES; NETHERLANDS; OPTIC ATROPHIES, HEREDITARY; POINT MUTATION; PREIMPLANTATION DIAGNOSIS;

EID: 0034255870     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(00)00101-2     Document Type: Article

References (2)

1. Poulton J, Marchington DR. Progress in genetic counselling and prenatal diagnosis of maternally inherited mtDNA diseases. Neuromusc Disord 2000 (submitted for publication).
2. White S., Collins V., R R.W., et al. Genetic counseling and prenatal diagnosis for the mitochondrial DNA mutations at nucleotide 8993. Am J Hum Genet. 65:1999;474-482.