TY  - GEN
AU  - de la Salle,H
AU  - Hanau,D
AU  - Fricker,D
AU  - Urlacher,A
AU  - Kelly,A
AU  - Salamero,J
AU  - Powis,S H
AU  - Donato,L
AU  - Bausinger,H
AU  - Laforet,M
TI  - Homozygous human TAP peptide transporter mutation in HLA class I deficiency
SN  - 0036-8075
PY  - 1994///0802
KW  - ATP Binding Cassette Transporter, Subfamily B, Member 2
KW  - ATP Binding Cassette Transporter, Subfamily B, Member 3
KW  - ATP-Binding Cassette Transporters
KW  - Adolescent
KW  - Amino Acid Sequence
KW  - Antigens, CD
KW  - analysis
KW  - Antigens, CD1
KW  - Base Sequence
KW  - Carrier Proteins
KW  - Child
KW  - Female
KW  - Histocompatibility Antigens Class I
KW  - Homozygote
KW  - Humans
KW  - Immunologic Deficiency Syndromes
KW  - genetics
KW  - Killer Cells, Natural
KW  - immunology
KW  - Langerhans Cells
KW  - Leukocyte Count
KW  - Lymphocytes
KW  - Male
KW  - Molecular Sequence Data
KW  - Mutation
KW  - T-Lymphocyte Subsets
KW  - T-Lymphocytes, Cytotoxic
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1126/science.7517574
ER  -