A point mutation of the ED1 gene in a Japanese family with X-linked hypohidrotic ectodermal dysplasia
Penulis
: H. SEKIGUCHI, X. J. WANG, K. MINAGUCHI, & M. YAKUSHIJI
Penerbit
: Paediatric Dentistry
Ringkasan :X-linked hypohidrotic ectodermal dysplasia (EDA) is characterized by the hypoplasia or absence of hair, teeth and sweat glands.
Daftar copy :
No. |
Barcode |
Lokasi |
No. Rak |
Ketersediaan |
1 |
08195149 |
Ruang Referensi - Perpustakaan FKIK |
01 |
TIDAK DIPINJAMKAN |
Diproses dalam : 0.15152502059937 detik