Display Settings:

Format

Send to:

Choose Destination
    Ann Dermatol Venereol. 2011;138(4):362-3. Epub 2011 Feb 26.

    [Mutations of C16orf57 gene have been identified in the poikiloderma-neutropenia syndrome and in a specific subset of congenital dyskeratosis with normal-length telomeres].

    [Article in French]

    Source

    Service de dermatologie, hôpital Saint-Éloi, Montpellier, France. o-dereure@chu-montpellier.fr

    PMID:
    21497268
    [PubMed - indexed for MEDLINE]

      Supplemental Content

      Icon for Masson (France)

      Save items

      loading

      Recent activity

      Your browsing activity is empty.

      Activity recording is turned off.

      Turn recording back on

      See more...
      Write to the Help Desk