Sharing of PPT mutations between distinct clinical forms of neuronal ceroid lipofuscinoses in patients from Scotland [4]

Journal of Medical Genetics

Volumn 35, Issue 9, 1998, Pages 790-

  Munroe, P B ^a   Greene, N D E ^a   Leung, K Y ^a   Mole, S E ^a   Gardiner, R M ^a   Mitchison, H M ^a   Stephenson, J B P ^a   Crow, Y J ^a  

^a ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL FEATURE; GENE MUTATION; HUMAN; LETTER; NEURONAL CEROID LIPOFUSCINOSIS; PRIORITY JOURNAL; UNITED KINGDOM;

AGE OF ONSET; HUMANS; MUTATION; MUTATION, MISSENSE; NEURONAL CEROID-LIPOFUSCINOSES; SCOTLAND; THIOLESTER HYDROLASES;

EID: 0031847823     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (5)