(Q32143704)
English
xeroderma pigmentosum group A
xeroderma pigmentosum characterized by involvement of the central and peripheral nervous systems in addition to cutaneous lesions that has material basis in caused by homozygous or compound heterozygous mutation in the XPA gene on chromosome 9q22
- XP group A
- xeroderma pigmentosum 1
- xeroderma pigmentosum complementation group A
- XPA
- XP1
- xeroderma pigmentosum, complementation group A
- Xeroderma Pigmentosum, Complementation Group type a
- xeroderma pigmentosum group type A
- Xp, Group a
- XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA
- XP-A
Statements
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Identifiers
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