Piebaldism and neurofibromatosis type 1: Family report

Dermatology Online Journal

Volumn 16, Issue 1, 2010, Pages

  Duarte, Ana Filipa ^a,b   Mota, Alberto ^a,b   Baudrier, Teresa ^a   Morais, Paulo ^a,b   Santos, António ^a   Cerqueira, Rita ^c   Tavares, Purificação ^c   Azevedo, Filomena ^a  

^a HOSPITAL DE SÃO JOÃO   (Portugal)

^b Inst of Pharmacol and Therapeutics   (Portugal)

^c CGC GENETICS   (Portugal)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHILD; DEPIGMENTATION; DISEASE ASSOCIATION; GENE; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; HUMAN; HYPOPIGMENTATION; KIT GENE; LEUKODERMA; MALE; NEUROFIBROMATOSIS; PIEBALDISM; PRESCHOOL CHILD; AMINO ACID SUBSTITUTION; EXON; GENETIC HETEROGENEITY; GENETICS; LEARNING DISORDER; MISSENSE MUTATION; POINT MUTATION; TUMOR SUPPRESSOR GENE;

STEM CELL FACTOR RECEPTOR;

ADULT; AMINO ACID SUBSTITUTION; CHILD, PRESCHOOL; EXONS; GENES, NEUROFIBROMATOSIS 1; GENETIC HETEROGENEITY; HUMANS; LEARNING DISORDERS; MALE; MUTATION, MISSENSE; NEUROFIBROMATOSIS 1; PIEBALDISM; POINT MUTATION; PROTO-ONCOGENE PROTEINS C-KIT;

EID: 75749106626     PISSN: None     EISSN: 10872108     Source Type: Journal    
DOI: None     Document Type: Article

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