A-point-mutation-of-the-ED1-gene-in-a-Japanese-family-with-X-linked-hypohidrotic-ectodermal-dysplasia

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A point mutation of the ED1 gene in a Japanese family with X-linked hypohidrotic ectodermal dysplasia

Author

: H. SEKIGUCHI, X. J. WANG, K. MINAGUCHI, & M. YAKUSHIJI

Edition

: 15

Editor

Collation

Subject

Publisher

: Paediatric Dentistry

Year

: 2005

ISBN

Call Number

Summary :
X-linked hypohidrotic ectodermal dysplasia (EDA) is characterized by the hypoplasia or absence of hair, teeth and sweat glands.

Copies :

No.	Barcode	Location	No. Shelf	Availability
1	08195149	Ruang Referensi - Perpustakaan FKIK	01	TIDAK DIPINJAMKAN

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