Publication
| De Cock L, D'haenens E, Vantomme L, Backers L, Beyens A, Claes KB, De Clercq G, de Putter R, Kumps C, Schuermans N, Sourbron J, Syryn H, Tavernier S, Vanbelleghem E, Vanakker O, Vandekerckhove B, Van Damme T, Callewaert B, Dheedene A, Vergult S, Menten B, Cracking rare disorders: a new minimally invasive RNA-seq protocol NPJ genomic medicine10:45 2025 |
| PubMed ID: 40436861 |
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| Records Return:
(3)
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| Catalog ID | Sex | Family | Relationship | Description | Collection_Type_id |
| GM15704 | Female | 1830 | mother | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC | GM |
| GM14870 | Male | 1830 | proband | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC | GM |
| GM20377 | Male | | proband | CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2 | GM |
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