Oculocutaneous albinism type 2 with a P gene missense mutation in a patient with Angelman syndrome

Journal of Medical Genetics

Volumn 37, Issue 5, 2000, Pages 392-394

  Saitoh, S ^a   Oiso, N ^a   Wada, T ^a   Narazaki, O ^a   Fukai, K ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHROMOSOME 15Q; HAPPY PUPPET SYNDROME; HUMAN; LETTER; MALE; MISSENSE MUTATION; NEWBORN; OCULOCUTANEOUS ALBINISM; PRIORITY JOURNAL;

EID: 0034017934     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.37.5.392     Document Type: Letter

References (15)