Recent advances in the molecular basis of inherited skin diseases

[1] HERLITZS JUNCTIONAL EPIDERMOLYSIS-BULLOSA IS LINKED TO MUTATIONS IN THE GENE (LAMC2) FOR THE GAMMA-2 SUBUNIT OF NICEIN/KALININ (LAMININ-5) [J]. NATURE GENETICS, 1994, 6 (03) : 299 - 304

[2] A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellers [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (04) : 984 - 991

[3] Genomic organization of the human hairless gene (HR) and identification of a mutation underlying congenital atrichia in an Arab Palestinian family [J]. GENOMICS, 1999, 56 (02) : 141 - 148

[4] Alopecia universalis associated with a mutation in the human hairless gene [J]. SCIENCE, 1998, 279 (5351) : 720 - 724

[5] Autosomal recessive inheritance of erythrokeratoderma variabilis [J]. PEDIATRIC DERMATOLOGY, 1997, 14 (05) : 355 - 358

[6] Aminoglycoside antibiotics restore dystrophin function to skeletal muscles of mdx mice [J]. JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (04) : 375 - 381

[7] Basarab T, 1999, BRIT J DERMATOL, V140, P689

[8] EPIDERMOLYSIS-BULLOSA SIMPLEX - EVIDENCE IN 2 FAMILIES FOR KERATIN GENE ABNORMALITIES [J]. SCIENCE, 1991, 254 (5035) : 1202 - 1205

[9] Structure sand function of hemidesmosomes: More than simple adhesion complexes [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 112 (04) : 411 - 418

[10] MUTATION OF A TYPE-II KERATIN GENE (K6A) IN PACHYONYCHIA-CONGENITA [J]. NATURE GENETICS, 1995, 10 (03) : 363 - 365

[1] HERLITZS JUNCTIONAL EPIDERMOLYSIS-BULLOSA IS LINKED TO MUTATIONS IN THE GENE (LAMC2) FOR THE GAMMA-2 SUBUNIT OF NICEIN/KALININ (LAMININ-5) [J]. NATURE GENETICS, 1994, 6 (03) : 299 - 304

[2] A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellers [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (04) : 984 - 991

[3] Genomic organization of the human hairless gene (HR) and identification of a mutation underlying congenital atrichia in an Arab Palestinian family [J]. GENOMICS, 1999, 56 (02) : 141 - 148

[4] Alopecia universalis associated with a mutation in the human hairless gene [J]. SCIENCE, 1998, 279 (5351) : 720 - 724

[5] Autosomal recessive inheritance of erythrokeratoderma variabilis [J]. PEDIATRIC DERMATOLOGY, 1997, 14 (05) : 355 - 358

[6] Aminoglycoside antibiotics restore dystrophin function to skeletal muscles of mdx mice [J]. JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (04) : 375 - 381

[7] Basarab T, 1999, BRIT J DERMATOL, V140, P689

[8] EPIDERMOLYSIS-BULLOSA SIMPLEX - EVIDENCE IN 2 FAMILIES FOR KERATIN GENE ABNORMALITIES [J]. SCIENCE, 1991, 254 (5035) : 1202 - 1205

[9] Structure sand function of hemidesmosomes: More than simple adhesion complexes [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 112 (04) : 411 - 418

[10] MUTATION OF A TYPE-II KERATIN GENE (K6A) IN PACHYONYCHIA-CONGENITA [J]. NATURE GENETICS, 1995, 10 (03) : 363 - 365